Canonical Allele Identifier: CA397725990

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7128276G>C (hg19) ; chr17:g.7224957G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224957G>C , CM000679.2:g.7224957G>C	GRCh38
NC_000017.10:g.7128276G>C , CM000679.1:g.7128276G>C	GRCh37
NC_000017.9:g.7069000G>C	NCBI36
NG_007975.1:g.10124G>C
NG_008391.2:g.94C>G
NG_033038.1:g.14588C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1828G>C MANE Select	ENSP00000349297.5:p.Ala610Pro
ENST00000322910.9:c.*1783G>C	ENSP00000325395.5:n.*1783G>C
ENST00000350303.9:c.1762G>C	ENSP00000344152.5:p.Ala588Pro
ENST00000356839.9:c.1828G>C	ENSP00000349297.5:p.Ala610Pro
ENST00000542255.6:c.707G>C
ENST00000543245.6:c.1897G>C	ENSP00000438689.2:p.Ala633Pro
ENST00000578033.1:n.253G>C
ENST00000578319.5:n.409G>C
ENST00000578711.1:n.1453G>C
ENST00000578809.5:n.400G>C
ENST00000579425.5:n.944G>C
ENST00000579546.1:c.563G>C
ENST00000583848.5:c.194G>C	ENSP00000466487.1:n.194G>C
ENST00000583850.5:n.599G>C
ENST00000583858.5:c.759G>C
NM_000018.3:c.1828G>C	NP_000009.1:p.Ala610Pro
NM_001033859.2:c.1762G>C	NP_001029031.1:p.Ala588Pro
NM_001270447.1:c.1897G>C	NP_001257376.1:p.Ala633Pro
NM_001270448.1:c.1600G>C	NP_001257377.1:p.Ala534Pro
XM_006721516.2:c.1849G>C	XP_006721579.2:p.Ala617Pro
XM_011523829.1:c.1747G>C	XP_011522131.1:p.Ala583Pro
XM_011523830.1:c.1726G>C	XP_011522132.1:p.Ala576Pro
XR_934021.1:n.1931G>C
XR_934022.1:n.1837G>C
XR_934023.1:n.1858G>C
XM_006721516.3:c.1849G>C	XP_006721579.2:p.Ala617Pro
XM_011523829.2:c.1747G>C	XP_011522131.1:p.Ala583Pro
XM_011523830.2:c.1726G>C	XP_011522132.1:p.Ala576Pro
XM_024450741.1:c.1816G>C	XP_024306509.1:p.Ala606Pro
XR_934021.2:n.1883G>C
XR_934022.2:n.1789G>C
XR_934023.2:n.1810G>C
NM_000018.4:c.1828G>C MANE Select	NP_000009.1:p.Ala610Pro
NM_001033859.3:c.1762G>C	NP_001029031.1:p.Ala588Pro
NM_001270447.2:c.1897G>C	NP_001257376.1:p.Ala633Pro
NM_001270448.2:c.1600G>C	NP_001257377.1:p.Ala534Pro