Canonical Allele Identifier: CA8337934

Gene: ACADVL

Linked Data

• ClinVar Variation Id: 541717
• ClinVar RCV Id: RCV000652035
• dbSNP Id: rs779458466
• ExAC: 17:7126184 G / A
• gnomAD v2: 17-7126184-G-A
• gnomAD v3: 17-7222865-G-A
• gnomAD v4: 17-7222865-G-A
• MyVariant Identifiers: chr17:g.7126184G>A (hg19) ; chr17:g.7222865G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222865G>A , CM000679.2:g.7222865G>A	GRCh38
NC_000017.10:g.7126184G>A , CM000679.1:g.7126184G>A	GRCh37
NC_000017.9:g.7066908G>A	NCBI36
NG_007975.1:g.8032G>A
NG_008391.2:g.2186C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1077G>A MANE Select	ENSP00000349297.5:p.Ala359=
ENST00000322910.9:c.*1032G>A	ENSP00000325395.5:n.*1032G>A
ENST00000350303.9:c.1011G>A	ENSP00000344152.5:p.Ala337=
ENST00000356839.9:c.1077G>A	ENSP00000349297.5:p.Ala359=
ENST00000543245.6:c.1146G>A	ENSP00000438689.2:p.Ala382=
ENST00000578824.5:n.226G>A
ENST00000582379.1:n.461G>A
ENST00000583858.5:c.106G>A
ENST00000585203.6:n.18G>A
NM_000018.3:c.1077G>A	NP_000009.1:p.Ala359=
NM_001033859.2:c.1011G>A	NP_001029031.1:p.Ala337=
NM_001270447.1:c.1146G>A	NP_001257376.1:p.Ala382=
NM_001270448.1:c.849G>A	NP_001257377.1:p.Ala283=
XM_006721516.2:c.1077G>A	XP_006721579.2:p.Ala359=
XM_011523829.1:c.1077G>A	XP_011522131.1:p.Ala359=
XM_011523830.1:c.1077G>A	XP_011522132.1:p.Ala359=
XR_934021.1:n.1184G>A
XR_934022.1:n.1184G>A
XR_934023.1:n.1184G>A
XM_006721516.3:c.1077G>A	XP_006721579.2:p.Ala359=
XM_011523829.2:c.1077G>A	XP_011522131.1:p.Ala359=
XM_011523830.2:c.1077G>A	XP_011522132.1:p.Ala359=
XM_024450741.1:c.1077G>A	XP_024306509.1:p.Ala359=
XR_934021.2:n.1136G>A
XR_934022.2:n.1136G>A
XR_934023.2:n.1136G>A
NM_000018.4:c.1077G>A MANE Select	NP_000009.1:p.Ala359=
NM_001033859.3:c.1011G>A	NP_001029031.1:p.Ala337=
NM_001270447.2:c.1146G>A	NP_001257376.1:p.Ala382=
NM_001270448.2:c.849G>A	NP_001257377.1:p.Ala283=