Canonical Allele Identifier: CA2245699185

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220949A= , CM000679.2:g.7220949A=	GRCh38
NC_000017.10:g.7124268A= , CM000679.1:g.7124268A=	GRCh37
NC_000017.9:g.7064992A=	NCBI36
NG_007975.1:g.6116A=
NG_008391.2:g.4102T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.368A= MANE Select	ENSP00000349297.5:p.Asp123=
ENST00000322910.9:c.*323A=	ENSP00000325395.5:n.*323A=
ENST00000350303.9:c.302A=	ENSP00000344152.5:p.Asp101=
ENST00000356839.9:c.368A=	ENSP00000349297.5:p.Asp123=
ENST00000543245.6:c.437A=	ENSP00000438689.2:p.Asp146=
ENST00000577191.5:n.445A=
ENST00000577433.5:n.576A=
ENST00000577857.5:n.293+119A=
ENST00000579286.5:n.549A=
ENST00000579886.2:c.206A=	ENSP00000463246.1:p.Asp69=
ENST00000580365.1:n.99A=
ENST00000581378.5:c.67A=
ENST00000581562.5:n.415A=
ENST00000582056.5:n.551A=
ENST00000582166.1:n.349A=
ENST00000583312.5:c.368A=	ENSP00000467920.1:p.Asp123=
ENST00000584103.5:c.401A=	ENSP00000465353.1:p.Asp134=
NM_000018.3:c.368A=	NP_000009.1:p.Asp123=
NM_001033859.2:c.302A=	NP_001029031.1:p.Asp101=
NM_001270447.1:c.437A=	NP_001257376.1:p.Asp146=
NM_001270448.1:c.140A=	NP_001257377.1:p.Asp47=
XM_006721516.2:c.368A=	XP_006721579.2:p.Asp123=
XM_011523829.1:c.368A=	XP_011522131.1:p.Asp123=
XM_011523830.1:c.368A=	XP_011522132.1:p.Asp123=
XR_934021.1:n.475A=
XR_934022.1:n.475A=
XR_934023.1:n.475A=
XM_006721516.3:c.368A=	XP_006721579.2:p.Asp123=
XM_011523829.2:c.368A=	XP_011522131.1:p.Asp123=
XM_011523830.2:c.368A=	XP_011522132.1:p.Asp123=
XM_024450741.1:c.368A=	XP_024306509.1:p.Asp123=
XR_934021.2:n.427A=
XR_934022.2:n.427A=
XR_934023.2:n.427A=
NM_000018.4:c.368A= MANE Select	NP_000009.1:p.Asp123=
NM_001033859.3:c.302A=	NP_001029031.1:p.Asp101=
NM_001270447.2:c.437A=	NP_001257376.1:p.Asp146=
NM_001270448.2:c.140A=	NP_001257377.1:p.Asp47=