Canonical Allele Identifier: CA2245714601

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224544G= , CM000679.2:g.7224544G=	GRCh38
NC_000017.10:g.7127863G= , CM000679.1:g.7127863G=	GRCh37
NC_000017.9:g.7068587G=	NCBI36
NG_007975.1:g.9711G=
NG_008391.2:g.507C=
NG_033038.1:g.15001C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356839.10:c.1670G= MANE Select	ENSP00000349297.5:p.Gly557=
ENST00000322910.9:c.*1625G=	ENSP00000325395.5:n.*1625G=
ENST00000350303.9:c.1604G=	ENSP00000344152.5:p.Gly535=
ENST00000356839.9:c.1670G=	ENSP00000349297.5:p.Gly557=
ENST00000542255.6:c.528G=
ENST00000543245.6:c.1739G=	ENSP00000438689.2:p.Gly580=
ENST00000578319.5:n.251G=
ENST00000578711.1:n.1040G=
ENST00000578809.5:n.242G=
ENST00000579391.1:n.274G=
ENST00000579425.5:n.786G=
ENST00000579546.1:c.405G=
ENST00000582450.1:n.178G=
ENST00000583074.5:n.291G=
ENST00000583848.5:c.56G=	ENSP00000466487.1:p.Gly19=
ENST00000583850.5:n.441G=
ENST00000583858.5:c.601G=
ENST00000585203.6:n.861G=
NM_000018.3:c.1670G=	NP_000009.1:p.Gly557=
NM_001033859.2:c.1604G=	NP_001029031.1:p.Gly535=
NM_001270447.1:c.1739G=	NP_001257376.1:p.Gly580=
NM_001270448.1:c.1442G=	NP_001257377.1:p.Gly481=
XM_006721516.2:c.1670G=	XP_006721579.2:p.Gly557=
XM_011523829.1:c.1568G=	XP_011522131.1:p.Gly523=
XM_011523830.1:c.1568G=	XP_011522132.1:p.Gly523=
XR_934021.1:n.1773G=
XR_934022.1:n.1679G=
XR_934023.1:n.1679G=
XM_006721516.3:c.1670G=	XP_006721579.2:p.Gly557=
XM_011523829.2:c.1568G=	XP_011522131.1:p.Gly523=
XM_011523830.2:c.1568G=	XP_011522132.1:p.Gly523=
XM_024450741.1:c.1658G=	XP_024306509.1:p.Gly553=
XR_934021.2:n.1725G=
XR_934022.2:n.1631G=
XR_934023.2:n.1631G=
NM_000018.4:c.1670G= MANE Select	NP_000009.1:p.Gly557=
NM_001033859.3:c.1604G=	NP_001029031.1:p.Gly535=
NM_001270447.2:c.1739G=	NP_001257376.1:p.Gly580=
NM_001270448.2:c.1442G=	NP_001257377.1:p.Gly481=