Canonical Allele Identifier: CA2245699087

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7220846G= , CM000679.2:g.7220846G=	GRCh38
NC_000017.10:g.7124165G= , CM000679.1:g.7124165G=	GRCh37
NC_000017.9:g.7064889G=	NCBI36
NG_007975.1:g.6013G=
NG_008391.2:g.4205C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.342+16G= MANE Select	ENSP00000349297.5:n.342+16G=
ENST00000322910.9:c.*297+16G=	ENSP00000325395.5:n.*297+16G=
ENST00000350303.9:c.276+16G=	ENSP00000344152.5:n.276+16G=
ENST00000356839.9:c.342+16G=	ENSP00000349297.5:n.342+16G=
ENST00000543245.6:c.411+16G=	ENSP00000438689.2:n.411+16G=
ENST00000577191.5:n.419+16G=
ENST00000577433.5:n.550+16G=
ENST00000577857.5:n.293+16G=
ENST00000579286.5:n.523+16G=
ENST00000579886.2:c.202-99G=	ENSP00000463246.1:n.202-99G=
ENST00000580365.1:n.73+16G=
ENST00000581378.5:c.41+16G=
ENST00000581562.5:n.389+16G=
ENST00000582056.5:n.448G=
ENST00000582166.1:n.246G=
ENST00000582356.5:n.557G=
ENST00000583312.5:c.342+16G=	ENSP00000467920.1:n.342+16G=
ENST00000584103.5:c.342+16G=	ENSP00000465353.1:n.342+16G=
NM_000018.3:c.342+16G=	NP_000009.1:n.342+16G=
NM_001033859.2:c.276+16G=	NP_001029031.1:n.276+16G=
NM_001270447.1:c.411+16G=	NP_001257376.1:n.411+16G=
NM_001270448.1:c.114+16G=	NP_001257377.1:n.114+16G=
XM_006721516.2:c.342+16G=	XP_006721579.2:n.342+16G=
XM_011523829.1:c.342+16G=	XP_011522131.1:n.342+16G=
XM_011523830.1:c.342+16G=	XP_011522132.1:n.342+16G=
XR_934021.1:n.449+16G=
XR_934022.1:n.449+16G=
XR_934023.1:n.449+16G=
XM_006721516.3:c.342+16G=	XP_006721579.2:n.342+16G=
XM_011523829.2:c.342+16G=	XP_011522131.1:n.342+16G=
XM_011523830.2:c.342+16G=	XP_011522132.1:n.342+16G=
XM_024450741.1:c.342+16G=	XP_024306509.1:n.342+16G=
XR_934021.2:n.401+16G=
XR_934022.2:n.401+16G=
XR_934023.2:n.401+16G=
NM_000018.4:c.342+16G= MANE Select	NP_000009.1:n.342+16G=
NM_001033859.3:c.276+16G=	NP_001029031.1:n.276+16G=
NM_001270447.2:c.411+16G=	NP_001257376.1:n.411+16G=
NM_001270448.2:c.114+16G=	NP_001257377.1:n.114+16G=