Canonical Allele Identifier: CA8337606

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220637G>C , CM000679.2:g.7220637G>C	GRCh38
NC_000017.10:g.7123956G>C , CM000679.1:g.7123956G>C	GRCh37
NC_000017.9:g.7064680G>C	NCBI36
NG_007975.1:g.5804G>C
NG_008391.2:g.4414C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000018.4:c.238G>C MANE Select	NP_000009.1:p.Gly80Arg
ENST00000356839.10:c.238G>C MANE Select	ENSP00000349297.5:p.Gly80Arg
NM_000018.3:c.238G>C	NP_000009.1:p.Gly80Arg
NM_001033859.2:c.172G>C	NP_001029031.1:p.Gly58Arg
NM_001033859.3:c.172G>C	NP_001029031.1:p.Gly58Arg
NM_001270447.1:c.307G>C	NP_001257376.1:p.Gly103Arg
NM_001270447.2:c.307G>C	NP_001257376.1:p.Gly103Arg
NM_001270448.1:c.10G>C	NP_001257377.1:p.Gly4Arg
NM_001270448.2:c.10G>C	NP_001257377.1:p.Gly4Arg
ENST00000322910.9:c.*193G>C	ENSP00000325395.5:n.*193G>C
ENST00000350303.9:c.172G>C	ENSP00000344152.5:p.Gly58Arg
ENST00000356839.9:c.238G>C	ENSP00000349297.5:p.Gly80Arg
ENST00000543245.6:c.307G>C	ENSP00000438689.2:p.Gly103Arg
ENST00000577191.5:n.315G>C
ENST00000577433.5:n.446G>C
ENST00000577857.5:n.229-129G>C
ENST00000578269.5:n.685G>C
ENST00000578421.1:n.446G>C
ENST00000579286.5:n.419G>C
ENST00000579886.2:c.201+111G>C	ENSP00000463246.1:n.201+111G>C
ENST00000580263.5:n.402G>C
ENST00000581562.5:n.285G>C
ENST00000582056.5:n.328G>C
ENST00000582166.1:n.126G>C
ENST00000582356.5:n.437G>C
ENST00000583312.5:c.238G>C	ENSP00000467920.1:p.Gly80Arg
ENST00000584103.5:c.238G>C	ENSP00000465353.1:p.Gly80Arg
XM_006721516.2:c.238G>C	XP_006721579.2:p.Gly80Arg
XM_006721516.3:c.238G>C	XP_006721579.2:p.Gly80Arg
XM_011523829.1:c.238G>C	XP_011522131.1:p.Gly80Arg
XM_011523829.2:c.238G>C	XP_011522131.1:p.Gly80Arg
XM_011523830.1:c.238G>C	XP_011522132.1:p.Gly80Arg
XM_011523830.2:c.238G>C	XP_011522132.1:p.Gly80Arg
XM_024450741.1:c.238G>C	XP_024306509.1:p.Gly80Arg
XR_934021.1:n.345G>C
XR_934021.2:n.297G>C
XR_934022.1:n.345G>C
XR_934022.2:n.297G>C
XR_934023.1:n.345G>C
XR_934023.2:n.297G>C