Canonical Allele Identifier: CA497694508

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7128278T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224959T>C , CM000679.2:g.7224959T>C	GRCh38
NC_000017.10:g.7128278T>C , CM000679.1:g.7128278T>C	GRCh37
NC_000017.9:g.7069002T>C	NCBI36
NG_007975.1:g.10126T>C
NG_008391.2:g.92A>G
NG_033038.1:g.14586A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1830T>C MANE Select	ENSP00000349297.5:p.Ala610=
ENST00000322910.9:c.*1785T>C	ENSP00000325395.5:n.*1785T>C
ENST00000350303.9:c.1764T>C	ENSP00000344152.5:p.Ala588=
ENST00000356839.9:c.1830T>C	ENSP00000349297.5:p.Ala610=
ENST00000542255.6:c.709T>C
ENST00000543245.6:c.1899T>C	ENSP00000438689.2:p.Ala633=
ENST00000578033.1:n.255T>C
ENST00000578319.5:n.411T>C
ENST00000578711.1:n.1455T>C
ENST00000578809.5:n.402T>C
ENST00000579425.5:n.946T>C
ENST00000579546.1:c.565T>C
ENST00000583848.5:c.196T>C	ENSP00000466487.1:n.196T>C
ENST00000583850.5:n.601T>C
ENST00000583858.5:c.761T>C
NM_000018.3:c.1830T>C	NP_000009.1:p.Ala610=
NM_001033859.2:c.1764T>C	NP_001029031.1:p.Ala588=
NM_001270447.1:c.1899T>C	NP_001257376.1:p.Ala633=
NM_001270448.1:c.1602T>C	NP_001257377.1:p.Ala534=
XM_006721516.2:c.1851T>C	XP_006721579.2:p.Ala617=
XM_011523829.1:c.1749T>C	XP_011522131.1:p.Ala583=
XM_011523830.1:c.1728T>C	XP_011522132.1:p.Ala576=
XR_934021.1:n.1933T>C
XR_934022.1:n.1839T>C
XR_934023.1:n.1860T>C
XM_006721516.3:c.1851T>C	XP_006721579.2:p.Ala617=
XM_011523829.2:c.1749T>C	XP_011522131.1:p.Ala583=
XM_011523830.2:c.1728T>C	XP_011522132.1:p.Ala576=
XM_024450741.1:c.1818T>C	XP_024306509.1:p.Ala606=
XR_934021.2:n.1885T>C
XR_934022.2:n.1791T>C
XR_934023.2:n.1812T>C
NM_000018.4:c.1830T>C MANE Select	NP_000009.1:p.Ala610=
NM_001033859.3:c.1764T>C	NP_001029031.1:p.Ala588=
NM_001270447.2:c.1899T>C	NP_001257376.1:p.Ala633=
NM_001270448.2:c.1602T>C	NP_001257377.1:p.Ala534=