Canonical Allele Identifier: CA2245699649

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7221328T= , CM000679.2:g.7221328T=	GRCh38
NC_000017.10:g.7124647T= , CM000679.1:g.7124647T=	GRCh37
NC_000017.9:g.7065371T=	NCBI36
NG_007975.1:g.6495T=
NG_008391.2:g.3723A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.478-210T= MANE Select	ENSP00000349297.5:n.478-210T=
ENST00000322910.9:c.*433-210T=	ENSP00000325395.5:n.*433-210T=
ENST00000350303.9:c.412-210T=	ENSP00000344152.5:n.412-210T=
ENST00000356839.9:c.478-210T=	ENSP00000349297.5:n.478-210T=
ENST00000543245.6:c.547-210T=	ENSP00000438689.2:n.547-210T=
ENST00000577191.5:n.555-210T=
ENST00000577433.5:n.686-210T=
ENST00000577857.5:n.294-210T=
ENST00000579286.5:n.659-210T=
ENST00000579886.2:c.316-210T=	ENSP00000463246.1:n.316-210T=
ENST00000580365.1:n.209-210T=
ENST00000581378.5:c.177-191T=
ENST00000581562.5:n.524+270T=
ENST00000582166.1:n.459-210T=
ENST00000583312.5:c.478-210T=	ENSP00000467920.1:n.478-210T=
ENST00000583760.1:n.50T=
NM_000018.3:c.478-210T=	NP_000009.1:n.478-210T=
NM_001033859.2:c.412-210T=	NP_001029031.1:n.412-210T=
NM_001270447.1:c.547-210T=	NP_001257376.1:n.547-210T=
NM_001270448.1:c.250-210T=	NP_001257377.1:n.250-210T=
XM_006721516.2:c.478-210T=	XP_006721579.2:n.478-210T=
XM_011523829.1:c.478-210T=	XP_011522131.1:n.478-210T=
XM_011523830.1:c.478-210T=	XP_011522132.1:n.478-210T=
XR_934021.1:n.585-210T=
XR_934022.1:n.585-210T=
XR_934023.1:n.585-210T=
XM_006721516.3:c.478-210T=	XP_006721579.2:n.478-210T=
XM_011523829.2:c.478-210T=	XP_011522131.1:n.478-210T=
XM_011523830.2:c.478-210T=	XP_011522132.1:n.478-210T=
XM_024450741.1:c.478-210T=	XP_024306509.1:n.478-210T=
XR_934021.2:n.537-210T=
XR_934022.2:n.537-210T=
XR_934023.2:n.537-210T=
NM_000018.4:c.478-210T= MANE Select	NP_000009.1:n.478-210T=
NM_001033859.3:c.412-210T=	NP_001029031.1:n.412-210T=
NM_001270447.2:c.547-210T=	NP_001257376.1:n.547-210T=
NM_001270448.2:c.250-210T=	NP_001257377.1:n.250-210T=