Canonical Allele Identifier: CA397726214

Gene: ACADVL

Linked Data

• MyVariant Identifiers: chr17:g.7128384G>C (hg19) ; chr17:g.7225065G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7225065G>C , CM000679.2:g.7225065G>C	GRCh38
NC_000017.10:g.7128384G>C , CM000679.1:g.7128384G>C	GRCh37
NC_000017.9:g.7069108G>C	NCBI36
NG_007975.1:g.10232G>C
NG_033038.1:g.14480C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1936G>C MANE Select	ENSP00000349297.5:p.Gly646Arg
ENST00000322910.9:c.*1891G>C	ENSP00000325395.5:n.*1891G>C
ENST00000350303.9:c.1870G>C	ENSP00000344152.5:p.Gly624Arg
ENST00000356839.9:c.1936G>C	ENSP00000349297.5:p.Gly646Arg
ENST00000542255.6:c.815G>C
ENST00000543245.6:c.2005G>C	ENSP00000438689.2:p.Gly669Arg
ENST00000578033.1:n.361G>C
ENST00000578319.5:n.517G>C
ENST00000578711.1:n.1561G>C
ENST00000578809.5:n.508G>C
ENST00000579425.5:n.1052G>C
ENST00000583848.5:c.302G>C	ENSP00000466487.1:n.302G>C
ENST00000583850.5:n.707G>C
ENST00000583858.5:c.867G>C
NM_000018.3:c.1936G>C	NP_000009.1:p.Gly646Arg
NM_001033859.2:c.1870G>C	NP_001029031.1:p.Gly624Arg
NM_001270447.1:c.2005G>C	NP_001257376.1:p.Gly669Arg
NM_001270448.1:c.1708G>C	NP_001257377.1:p.Gly570Arg
XM_006721516.2:c.1957G>C	XP_006721579.2:p.Gly653Arg
XM_011523829.1:c.1855G>C	XP_011522131.1:p.Gly619Arg
XM_011523830.1:c.1834G>C	XP_011522132.1:p.Gly612Arg
XR_934021.1:n.2039G>C
XR_934022.1:n.1945G>C
XR_934023.1:n.1966G>C
XM_006721516.3:c.1957G>C	XP_006721579.2:p.Gly653Arg
XM_011523829.2:c.1855G>C	XP_011522131.1:p.Gly619Arg
XM_011523830.2:c.1834G>C	XP_011522132.1:p.Gly612Arg
XM_024450741.1:c.1924G>C	XP_024306509.1:p.Gly642Arg
XR_934021.2:n.1991G>C
XR_934022.2:n.1897G>C
XR_934023.2:n.1918G>C
NM_000018.4:c.1936G>C MANE Select	NP_000009.1:p.Gly646Arg
NM_001033859.3:c.1870G>C	NP_001029031.1:p.Gly624Arg
NM_001270447.2:c.2005G>C	NP_001257376.1:p.Gly669Arg
NM_001270448.2:c.1708G>C	NP_001257377.1:p.Gly570Arg