Canonical Allele Identifier: CA287437399
Gene: ACADVL HGNC NCBI

Linked Data

ClinVar Variation Id: 1203085
ClinVar RCV Id: RCV001569001
dbSNP Id: rs114612853
gnomAD v2: 17-7125907-T-C
gnomAD v3: 17-7222588-T-C
gnomAD v4: 17-7222588-T-C
MyVariant Identifiers: chr17:g.7125907T>C (hg19) chr17:g.7222588T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222588T>C , CM000679.2:g.7222588T>C GRCh38
NC_000017.10:g.7125907T>C , CM000679.1:g.7125907T>C GRCh37
NC_000017.9:g.7066631T>C NCBI36
NG_007975.1:g.7755T>C
NG_008391.2:g.2463A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.879-79T>C MANE Select ENSP00000349297.5:n.879-79T>C
ENST00000322910.9:c.*834-79T>C ENSP00000325395.5:n.*834-79T>C
ENST00000350303.9:c.813-79T>C ENSP00000344152.5:n.813-79T>C
ENST00000356839.9:c.879-79T>C ENSP00000349297.5:n.879-79T>C
ENST00000543245.6:c.948-79T>C ENSP00000438689.2:n.948-79T>C
ENST00000581378.5:c.597-79T>C
ENST00000582379.1:n.263-79T>C
NM_000018.3:c.879-79T>C NP_000009.1:n.879-79T>C
NM_001033859.2:c.813-79T>C NP_001029031.1:n.813-79T>C
NM_001270447.1:c.948-79T>C NP_001257376.1:n.948-79T>C
NM_001270448.1:c.651-79T>C NP_001257377.1:n.651-79T>C
XM_006721516.2:c.879-79T>C XP_006721579.2:n.879-79T>C
XM_011523829.1:c.879-79T>C XP_011522131.1:n.879-79T>C
XM_011523830.1:c.879-79T>C XP_011522132.1:n.879-79T>C
XR_934021.1:n.986-79T>C
XR_934022.1:n.986-79T>C
XR_934023.1:n.986-79T>C
XM_006721516.3:c.879-79T>C XP_006721579.2:n.879-79T>C
XM_011523829.2:c.879-79T>C XP_011522131.1:n.879-79T>C
XM_011523830.2:c.879-79T>C XP_011522132.1:n.879-79T>C
XM_024450741.1:c.879-79T>C XP_024306509.1:n.879-79T>C
XR_934021.2:n.938-79T>C
XR_934022.2:n.938-79T>C
XR_934023.2:n.938-79T>C
NM_000018.4:c.879-79T>C MANE Select NP_000009.1:n.879-79T>C
NM_001033859.3:c.813-79T>C NP_001029031.1:n.813-79T>C
NM_001270447.2:c.948-79T>C NP_001257376.1:n.948-79T>C
NM_001270448.2:c.651-79T>C NP_001257377.1:n.651-79T>C
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