Canonical Allele Identifier: CA397724359

Gene: ACADVL

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223158A>G , CM000679.2:g.7223158A>G	GRCh38
NC_000017.10:g.7126477A>G , CM000679.1:g.7126477A>G	GRCh37
NC_000017.9:g.7067201A>G	NCBI36
NG_007975.1:g.8325A>G
NG_008391.2:g.1893T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1103A>G MANE Select	ENSP00000349297.5:p.Gln368Arg
ENST00000322910.9:c.*1058A>G	ENSP00000325395.5:n.*1058A>G
ENST00000350303.9:c.1037A>G	ENSP00000344152.5:p.Gln346Arg
ENST00000356839.9:c.1103A>G	ENSP00000349297.5:p.Gln368Arg
ENST00000543245.6:c.1172A>G	ENSP00000438689.2:p.Gln391Arg
ENST00000578579.2:n.52A>G
ENST00000578824.5:n.519A>G
ENST00000579425.5:n.127A>G
ENST00000582379.1:n.754A>G
ENST00000583858.5:c.132A>G
ENST00000585203.6:n.311A>G
NM_000018.3:c.1103A>G	NP_000009.1:p.Gln368Arg
NM_001033859.2:c.1037A>G	NP_001029031.1:p.Gln346Arg
NM_001270447.1:c.1172A>G	NP_001257376.1:p.Gln391Arg
NM_001270448.1:c.875A>G	NP_001257377.1:p.Gln292Arg
XM_006721516.2:c.1103A>G	XP_006721579.2:p.Gln368Arg
XM_011523829.1:c.1103A>G	XP_011522131.1:p.Gln368Arg
XM_011523830.1:c.1103A>G	XP_011522132.1:p.Gln368Arg
XR_934021.1:n.1210A>G
XR_934022.1:n.1210A>G
XR_934023.1:n.1210A>G
XM_006721516.3:c.1103A>G	XP_006721579.2:p.Gln368Arg
XM_011523829.2:c.1103A>G	XP_011522131.1:p.Gln368Arg
XM_011523830.2:c.1103A>G	XP_011522132.1:p.Gln368Arg
XM_024450741.1:c.1103A>G	XP_024306509.1:p.Gln368Arg
XR_934021.2:n.1162A>G
XR_934022.2:n.1162A>G
XR_934023.2:n.1162A>G
NM_000018.4:c.1103A>G MANE Select	NP_000009.1:p.Gln368Arg
NM_001033859.3:c.1037A>G	NP_001029031.1:p.Gln346Arg
NM_001270447.2:c.1172A>G	NP_001257376.1:p.Gln391Arg
NM_001270448.2:c.875A>G	NP_001257377.1:p.Gln292Arg