Canonical Allele Identifier: CA2245709578

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7222772T= , CM000679.2:g.7222772T=	GRCh38
NC_000017.10:g.7126091T= , CM000679.1:g.7126091T=	GRCh37
NC_000017.9:g.7066815T=	NCBI36
NG_007975.1:g.7939T=
NG_008391.2:g.2279A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.984T= MANE Select	ENSP00000349297.5:p.Ser328=
ENST00000322910.9:c.*939T=	ENSP00000325395.5:n.*939T=
ENST00000350303.9:c.918T=	ENSP00000344152.5:p.Ser306=
ENST00000356839.9:c.984T=	ENSP00000349297.5:p.Ser328=
ENST00000543245.6:c.1053T=	ENSP00000438689.2:p.Ser351=
ENST00000578824.5:n.133T=
ENST00000581378.5:c.702T=
ENST00000582379.1:n.368T=
ENST00000583858.5:c.13T=
NM_000018.3:c.984T=	NP_000009.1:p.Ser328=
NM_001033859.2:c.918T=	NP_001029031.1:p.Ser306=
NM_001270447.1:c.1053T=	NP_001257376.1:p.Ser351=
NM_001270448.1:c.756T=	NP_001257377.1:p.Ser252=
XM_006721516.2:c.984T=	XP_006721579.2:p.Ser328=
XM_011523829.1:c.984T=	XP_011522131.1:p.Ser328=
XM_011523830.1:c.984T=	XP_011522132.1:p.Ser328=
XR_934021.1:n.1091T=
XR_934022.1:n.1091T=
XR_934023.1:n.1091T=
XM_006721516.3:c.984T=	XP_006721579.2:p.Ser328=
XM_011523829.2:c.984T=	XP_011522131.1:p.Ser328=
XM_011523830.2:c.984T=	XP_011522132.1:p.Ser328=
XM_024450741.1:c.984T=	XP_024306509.1:p.Ser328=
XR_934021.2:n.1043T=
XR_934022.2:n.1043T=
XR_934023.2:n.1043T=
NM_000018.4:c.984T= MANE Select	NP_000009.1:p.Ser328=
NM_001033859.3:c.918T=	NP_001029031.1:p.Ser306=
NM_001270447.2:c.1053T=	NP_001257376.1:p.Ser351=
NM_001270448.2:c.756T=	NP_001257377.1:p.Ser252=