Canonical Allele Identifier: CA2245711399
Gene: ACADVL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223641C= , CM000679.2:g.7223641C= GRCh38
NC_000017.10:g.7126960C= , CM000679.1:g.7126960C= GRCh37
NC_000017.9:g.7067684C= NCBI36
NG_007975.1:g.8808C=
NG_008391.2:g.1410G=
NG_033038.1:g.15904G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1183-3C= MANE Select ENSP00000349297.5:n.1183-3C=
ENST00000322910.9:c.*1138-3C= ENSP00000325395.5:n.*1138-3C=
ENST00000350303.9:c.1117-3C= ENSP00000344152.5:n.1117-3C=
ENST00000356839.9:c.1183-3C= ENSP00000349297.5:n.1183-3C=
ENST00000542255.6:c.41-3C=
ENST00000543245.6:c.1252-3C= ENSP00000438689.2:n.1252-3C=
ENST00000578579.2:n.351C=
ENST00000578711.1:n.137C=
ENST00000578824.5:n.599-3C=
ENST00000579425.5:n.207-3C=
ENST00000579546.1:c.20-3C=
ENST00000583858.5:c.212-3C=
ENST00000585203.6:n.391-3C=
NM_000018.3:c.1183-3C= NP_000009.1:n.1183-3C=
NM_001033859.2:c.1117-3C= NP_001029031.1:n.1117-3C=
NM_001270447.1:c.1252-3C= NP_001257376.1:n.1252-3C=
NM_001270448.1:c.955-3C= NP_001257377.1:n.955-3C=
XM_006721516.2:c.1183-3C= XP_006721579.2:n.1183-3C=
XM_011523829.1:c.1183-3C= XP_011522131.1:n.1183-3C=
XM_011523830.1:c.1183-3C= XP_011522132.1:n.1183-3C=
XR_934021.1:n.1290-3C=
XR_934022.1:n.1290-3C=
XR_934023.1:n.1290-3C=
XM_006721516.3:c.1183-3C= XP_006721579.2:n.1183-3C=
XM_011523829.2:c.1183-3C= XP_011522131.1:n.1183-3C=
XM_011523830.2:c.1183-3C= XP_011522132.1:n.1183-3C=
XM_024450741.1:c.1183-3C= XP_024306509.1:n.1183-3C=
XR_934021.2:n.1242-3C=
XR_934022.2:n.1242-3C=
XR_934023.2:n.1242-3C=
NM_000018.4:c.1183-3C= MANE Select NP_000009.1:n.1183-3C=
NM_001033859.3:c.1117-3C= NP_001029031.1:n.1117-3C=
NM_001270447.2:c.1252-3C= NP_001257376.1:n.1252-3C=
NM_001270448.2:c.955-3C= NP_001257377.1:n.955-3C=
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