Canonical Allele Identifier: CA2245698638

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220654T= , CM000679.2:g.7220654T=	GRCh38
NC_000017.10:g.7123973T= , CM000679.1:g.7123973T=	GRCh37
NC_000017.9:g.7064697T=	NCBI36
NG_007975.1:g.5821T=
NG_008391.2:g.4397A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.255T= MANE Select	ENSP00000349297.5:p.Asp85=
ENST00000322910.9:c.*210T=	ENSP00000325395.5:n.*210T=
ENST00000350303.9:c.189T=	ENSP00000344152.5:p.Asp63=
ENST00000356839.9:c.255T=	ENSP00000349297.5:p.Asp85=
ENST00000543245.6:c.324T=	ENSP00000438689.2:p.Asp108=
ENST00000577191.5:n.332T=
ENST00000577433.5:n.463T=
ENST00000577857.5:n.229-112T=
ENST00000578269.5:n.702T=
ENST00000578421.1:n.463T=
ENST00000579286.5:n.436T=
ENST00000579886.2:c.201+128T=	ENSP00000463246.1:n.201+128T=
ENST00000580263.5:n.419T=
ENST00000581562.5:n.302T=
ENST00000582056.5:n.345T=
ENST00000582166.1:n.143T=
ENST00000582356.5:n.454T=
ENST00000583312.5:c.255T=	ENSP00000467920.1:p.Asp85=
ENST00000584103.5:c.255T=	ENSP00000465353.1:p.Asp85=
NM_000018.3:c.255T=	NP_000009.1:p.Asp85=
NM_001033859.2:c.189T=	NP_001029031.1:p.Asp63=
NM_001270447.1:c.324T=	NP_001257376.1:p.Asp108=
NM_001270448.1:c.27T=	NP_001257377.1:p.Asp9=
XM_006721516.2:c.255T=	XP_006721579.2:p.Asp85=
XM_011523829.1:c.255T=	XP_011522131.1:p.Asp85=
XM_011523830.1:c.255T=	XP_011522132.1:p.Asp85=
XR_934021.1:n.362T=
XR_934022.1:n.362T=
XR_934023.1:n.362T=
XM_006721516.3:c.255T=	XP_006721579.2:p.Asp85=
XM_011523829.2:c.255T=	XP_011522131.1:p.Asp85=
XM_011523830.2:c.255T=	XP_011522132.1:p.Asp85=
XM_024450741.1:c.255T=	XP_024306509.1:p.Asp85=
XR_934021.2:n.314T=
XR_934022.2:n.314T=
XR_934023.2:n.314T=
NM_000018.4:c.255T= MANE Select	NP_000009.1:p.Asp85=
NM_001033859.3:c.189T=	NP_001029031.1:p.Asp63=
NM_001270447.2:c.324T=	NP_001257376.1:p.Asp108=
NM_001270448.2:c.27T=	NP_001257377.1:p.Asp9=