Canonical Allele Identifier: CA2245708872
Gene: ACADVL HGNC NCBI

Linked Data

dbSNP Id: rs1597529409

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222546T>G , CM000679.2:g.7222546T>G GRCh38
NC_000017.10:g.7125865T>G , CM000679.1:g.7125865T>G GRCh37
NC_000017.9:g.7066589T>G NCBI36
NG_007975.1:g.7713T>G
NG_008391.2:g.2505A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.879-121T>G MANE Select ENSP00000349297.5:n.879-121T>G
ENST00000322910.9:c.*834-121T>G ENSP00000325395.5:n.*834-121T>G
ENST00000350303.9:c.813-121T>G ENSP00000344152.5:n.813-121T>G
ENST00000356839.9:c.879-121T>G ENSP00000349297.5:n.879-121T>G
ENST00000543245.6:c.948-121T>G ENSP00000438689.2:n.948-121T>G
ENST00000581378.5:c.597-121T>G
ENST00000582379.1:n.263-121T>G
NM_000018.3:c.879-121T>G NP_000009.1:n.879-121T>G
NM_001033859.2:c.813-121T>G NP_001029031.1:n.813-121T>G
NM_001270447.1:c.948-121T>G NP_001257376.1:n.948-121T>G
NM_001270448.1:c.651-121T>G NP_001257377.1:n.651-121T>G
XM_006721516.2:c.879-121T>G XP_006721579.2:n.879-121T>G
XM_011523829.1:c.879-121T>G XP_011522131.1:n.879-121T>G
XM_011523830.1:c.879-121T>G XP_011522132.1:n.879-121T>G
XR_934021.1:n.986-121T>G
XR_934022.1:n.986-121T>G
XR_934023.1:n.986-121T>G
XM_006721516.3:c.879-121T>G XP_006721579.2:n.879-121T>G
XM_011523829.2:c.879-121T>G XP_011522131.1:n.879-121T>G
XM_011523830.2:c.879-121T>G XP_011522132.1:n.879-121T>G
XM_024450741.1:c.879-121T>G XP_024306509.1:n.879-121T>G
XR_934021.2:n.938-121T>G
XR_934022.2:n.938-121T>G
XR_934023.2:n.938-121T>G
NM_000018.4:c.879-121T>G MANE Select NP_000009.1:n.879-121T>G
NM_001033859.3:c.813-121T>G NP_001029031.1:n.813-121T>G
NM_001270447.2:c.948-121T>G NP_001257376.1:n.948-121T>G
NM_001270448.2:c.651-121T>G NP_001257377.1:n.651-121T>G