Canonical Allele Identifier: CA774743158

Gene: ACADVL

Linked Data

• dbSNP Id: rs1231871770
• gnomAD v3: 17-7222610-T-A
• gnomAD v4: 17-7222610-T-A
• MyVariant Identifiers: chr17:g.7125929T>A (hg19) ; chr17:g.7222610T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222610T>A , CM000679.2:g.7222610T>A	GRCh38
NC_000017.10:g.7125929T>A , CM000679.1:g.7125929T>A	GRCh37
NC_000017.9:g.7066653T>A	NCBI36
NG_007975.1:g.7777T>A
NG_008391.2:g.2441A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.879-57T>A MANE Select	ENSP00000349297.5:n.879-57T>A
ENST00000322910.9:c.*834-57T>A	ENSP00000325395.5:n.*834-57T>A
ENST00000350303.9:c.813-57T>A	ENSP00000344152.5:n.813-57T>A
ENST00000356839.9:c.879-57T>A	ENSP00000349297.5:n.879-57T>A
ENST00000543245.6:c.948-57T>A	ENSP00000438689.2:n.948-57T>A
ENST00000581378.5:c.597-57T>A
ENST00000582379.1:n.263-57T>A
NM_000018.3:c.879-57T>A	NP_000009.1:n.879-57T>A
NM_001033859.2:c.813-57T>A	NP_001029031.1:n.813-57T>A
NM_001270447.1:c.948-57T>A	NP_001257376.1:n.948-57T>A
NM_001270448.1:c.651-57T>A	NP_001257377.1:n.651-57T>A
XM_006721516.2:c.879-57T>A	XP_006721579.2:n.879-57T>A
XM_011523829.1:c.879-57T>A	XP_011522131.1:n.879-57T>A
XM_011523830.1:c.879-57T>A	XP_011522132.1:n.879-57T>A
XR_934021.1:n.986-57T>A
XR_934022.1:n.986-57T>A
XR_934023.1:n.986-57T>A
XM_006721516.3:c.879-57T>A	XP_006721579.2:n.879-57T>A
XM_011523829.2:c.879-57T>A	XP_011522131.1:n.879-57T>A
XM_011523830.2:c.879-57T>A	XP_011522132.1:n.879-57T>A
XM_024450741.1:c.879-57T>A	XP_024306509.1:n.879-57T>A
XR_934021.2:n.938-57T>A
XR_934022.2:n.938-57T>A
XR_934023.2:n.938-57T>A
NM_000018.4:c.879-57T>A MANE Select	NP_000009.1:n.879-57T>A
NM_001033859.3:c.813-57T>A	NP_001029031.1:n.813-57T>A
NM_001270447.2:c.948-57T>A	NP_001257376.1:n.948-57T>A
NM_001270448.2:c.651-57T>A	NP_001257377.1:n.651-57T>A