Canonical Allele Identifier: CA397724579
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs1597533893
MyVariant Identifiers: chr17:g.7126979T>G (hg19) chr17:g.7223660T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223660T>G , CM000679.2:g.7223660T>G GRCh38
NC_000017.10:g.7126979T>G , CM000679.1:g.7126979T>G GRCh37
NC_000017.9:g.7067703T>G NCBI36
NG_007975.1:g.8827T>G
NG_008391.2:g.1391A>C
NG_033038.1:g.15885A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1199T>G MANE Select ENSP00000349297.5:p.Val400Gly
ENST00000322910.9:c.*1154T>G ENSP00000325395.5:n.*1154T>G
ENST00000350303.9:c.1133T>G ENSP00000344152.5:p.Val378Gly
ENST00000356839.9:c.1199T>G ENSP00000349297.5:p.Val400Gly
ENST00000542255.6:c.57T>G
ENST00000543245.6:c.1268T>G ENSP00000438689.2:p.Val423Gly
ENST00000578579.2:n.370T>G
ENST00000578711.1:n.156T>G
ENST00000578824.5:n.615T>G
ENST00000579425.5:n.223T>G
ENST00000579546.1:c.36T>G
ENST00000583858.5:c.228T>G
ENST00000585203.6:n.407T>G
NM_000018.3:c.1199T>G NP_000009.1:p.Val400Gly
NM_001033859.2:c.1133T>G NP_001029031.1:p.Val378Gly
NM_001270447.1:c.1268T>G NP_001257376.1:p.Val423Gly
NM_001270448.1:c.971T>G NP_001257377.1:p.Val324Gly
XM_006721516.2:c.1199T>G XP_006721579.2:p.Val400Gly
XM_011523829.1:c.1199T>G XP_011522131.1:p.Val400Gly
XM_011523830.1:c.1199T>G XP_011522132.1:p.Val400Gly
XR_934021.1:n.1306T>G
XR_934022.1:n.1306T>G
XR_934023.1:n.1306T>G
XM_006721516.3:c.1199T>G XP_006721579.2:p.Val400Gly
XM_011523829.2:c.1199T>G XP_011522131.1:p.Val400Gly
XM_011523830.2:c.1199T>G XP_011522132.1:p.Val400Gly
XM_024450741.1:c.1199T>G XP_024306509.1:p.Val400Gly
XR_934021.2:n.1258T>G
XR_934022.2:n.1258T>G
XR_934023.2:n.1258T>G
NM_000018.4:c.1199T>G MANE Select NP_000009.1:p.Val400Gly
NM_001033859.3:c.1133T>G NP_001029031.1:p.Val378Gly
NM_001270447.2:c.1268T>G NP_001257376.1:p.Val423Gly
NM_001270448.2:c.971T>G NP_001257377.1:p.Val324Gly
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