Canonical Allele Identifier: CA2635784480
Gene: ACADVL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7224512_7224513insTCCCTGGGGACA , CM000679.2:g.7224512_7224513insTCCCTGGGGACA GRCh38
NC_000017.10:g.7127831_7127832insTCCCTGGGGACA , CM000679.1:g.7127831_7127832insTCCCTGGGGACA GRCh37
NC_000017.9:g.7068555_7068556insTCCCTGGGGACA NCBI36
NG_007975.1:g.9679_9680insTCCCTGGGGACA
NG_008391.2:g.538_539insTGTCCCCAGGGA
NG_033038.1:g.15032_15033insTGTCCCCAGGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1638_1639insTCCCTGGGGACA MANE Select ENSP00000349297.5:p.Val546_Val547insSerLeuGlyThr
ENST00000322910.9:c.*1593_*1594insTCCCTGGGGACA ENSP00000325395.5:n.*1593_*1594insTCCCTGGGGACA
ENST00000350303.9:c.1572_1573insTCCCTGGGGACA ENSP00000344152.5:p.Val524_Val525insSerLeuGlyThr
ENST00000356839.9:c.1638_1639insTCCCTGGGGACA ENSP00000349297.5:p.Val546_Val547insSerLeuGlyThr
ENST00000542255.6:c.496_497insTCCCTGGGGACA
ENST00000543245.6:c.1707_1708insTCCCTGGGGACA ENSP00000438689.2:p.Val569_Val570insSerLeuGlyThr
ENST00000578319.5:n.219_220insTCCCTGGGGACA
ENST00000578711.1:n.1008_1009insTCCCTGGGGACA
ENST00000578809.5:n.210_211insTCCCTGGGGACA
ENST00000579391.1:n.242_243insTCCCTGGGGACA
ENST00000579425.5:n.754_755insTCCCTGGGGACA
ENST00000579546.1:c.373_374insTCCCTGGGGACA
ENST00000579894.5:n.425_426insTCCCTGGGGACA
ENST00000582450.1:n.146_147insTCCCTGGGGACA
ENST00000583074.5:n.259_260insTCCCTGGGGACA
ENST00000583848.5:c.24_25insTCCCTGGGGACA ENSP00000466487.1:p.Val8_Val9insSerLeuGlyThr
ENST00000583850.5:n.409_410insTCCCTGGGGACA
ENST00000583858.5:c.569_570insTCCCTGGGGACA
ENST00000585203.6:n.829_830insTCCCTGGGGACA
NM_000018.3:c.1638_1639insTCCCTGGGGACA NP_000009.1:p.Val546_Val547insSerLeuGlyThr
NM_001033859.2:c.1572_1573insTCCCTGGGGACA NP_001029031.1:p.Val524_Val525insSerLeuGlyThr
NM_001270447.1:c.1707_1708insTCCCTGGGGACA NP_001257376.1:p.Val569_Val570insSerLeuGlyThr
NM_001270448.1:c.1410_1411insTCCCTGGGGACA NP_001257377.1:p.Val470_Val471insSerLeuGlyThr
XM_006721516.2:c.1638_1639insTCCCTGGGGACA XP_006721579.2:p.Val546_Val547insSerLeuGlyThr
XM_011523829.1:c.1536_1537insTCCCTGGGGACA XP_011522131.1:p.Val512_Val513insSerLeuGlyThr
XM_011523830.1:c.1536_1537insTCCCTGGGGACA XP_011522132.1:p.Val512_Val513insSerLeuGlyThr
XR_934021.1:n.1741_1742insTCCCTGGGGACA
XR_934022.1:n.1647_1648insTCCCTGGGGACA
XR_934023.1:n.1647_1648insTCCCTGGGGACA
XM_006721516.3:c.1638_1639insTCCCTGGGGACA XP_006721579.2:p.Val546_Val547insSerLeuGlyThr
XM_011523829.2:c.1536_1537insTCCCTGGGGACA XP_011522131.1:p.Val512_Val513insSerLeuGlyThr
XM_011523830.2:c.1536_1537insTCCCTGGGGACA XP_011522132.1:p.Val512_Val513insSerLeuGlyThr
XM_024450741.1:c.1626_1627insTCCCTGGGGACA XP_024306509.1:p.Val542_Val543insSerLeuGlyThr
XR_934021.2:n.1693_1694insTCCCTGGGGACA
XR_934022.2:n.1599_1600insTCCCTGGGGACA
XR_934023.2:n.1599_1600insTCCCTGGGGACA
NM_000018.4:c.1638_1639insTCCCTGGGGACA MANE Select NP_000009.1:p.Val546_Val547insSerLeuGlyThr
NM_001033859.3:c.1572_1573insTCCCTGGGGACA NP_001029031.1:p.Val524_Val525insSerLeuGlyThr
NM_001270447.2:c.1707_1708insTCCCTGGGGACA NP_001257376.1:p.Val569_Val570insSerLeuGlyThr
NM_001270448.2:c.1410_1411insTCCCTGGGGACA NP_001257377.1:p.Val470_Val471insSerLeuGlyThr