Canonical Allele Identifier: CA2245700192

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221597G= , CM000679.2:g.7221597G=	GRCh38
NC_000017.10:g.7124916G= , CM000679.1:g.7124916G=	GRCh37
NC_000017.9:g.7065640G=	NCBI36
NG_007975.1:g.6764G=
NG_008391.2:g.3454C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.537G= MANE Select	ENSP00000349297.5:p.Gly179=
ENST00000322910.9:c.*492G=	ENSP00000325395.5:n.*492G=
ENST00000350303.9:c.471G=	ENSP00000344152.5:p.Gly157=
ENST00000356839.9:c.537G=	ENSP00000349297.5:p.Gly179=
ENST00000543245.6:c.606G=	ENSP00000438689.2:p.Gly202=
ENST00000577191.5:n.614G=
ENST00000577433.5:n.745G=
ENST00000577857.5:n.353G=
ENST00000579286.5:n.718G=
ENST00000579886.2:c.375G=	ENSP00000463246.1:p.Gly125=
ENST00000580365.1:n.268G=
ENST00000581378.5:c.255G=
ENST00000581562.5:n.525-355G=
ENST00000582166.1:n.518G=
ENST00000583312.5:c.537G=	ENSP00000467920.1:p.Gly179=
ENST00000583760.1:n.319G=
NM_000018.3:c.537G=	NP_000009.1:p.Gly179=
NM_001033859.2:c.471G=	NP_001029031.1:p.Gly157=
NM_001270447.1:c.606G=	NP_001257376.1:p.Gly202=
NM_001270448.1:c.309G=	NP_001257377.1:p.Gly103=
XM_006721516.2:c.537G=	XP_006721579.2:p.Gly179=
XM_011523829.1:c.537G=	XP_011522131.1:p.Gly179=
XM_011523830.1:c.537G=	XP_011522132.1:p.Gly179=
XR_934021.1:n.644G=
XR_934022.1:n.644G=
XR_934023.1:n.644G=
XM_006721516.3:c.537G=	XP_006721579.2:p.Gly179=
XM_011523829.2:c.537G=	XP_011522131.1:p.Gly179=
XM_011523830.2:c.537G=	XP_011522132.1:p.Gly179=
XM_024450741.1:c.537G=	XP_024306509.1:p.Gly179=
XR_934021.2:n.596G=
XR_934022.2:n.596G=
XR_934023.2:n.596G=
NM_000018.4:c.537G= MANE Select	NP_000009.1:p.Gly179=
NM_001033859.3:c.471G=	NP_001029031.1:p.Gly157=
NM_001270447.2:c.606G=	NP_001257376.1:p.Gly202=
NM_001270448.2:c.309G=	NP_001257377.1:p.Gly103=