Canonical Allele Identifier: CA2245714888

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224613C= , CM000679.2:g.7224613C=	GRCh38
NC_000017.10:g.7127932C= , CM000679.1:g.7127932C=	GRCh37
NC_000017.9:g.7068656C=	NCBI36
NG_007975.1:g.9780C=
NG_008391.2:g.438G=
NG_033038.1:g.14932G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1679-29C= MANE Select	ENSP00000349297.5:n.1679-29C=
ENST00000322910.9:c.*1634-29C=	ENSP00000325395.5:n.*1634-29C=
ENST00000350303.9:c.1613-29C=	ENSP00000344152.5:n.1613-29C=
ENST00000356839.9:c.1679-29C=	ENSP00000349297.5:n.1679-29C=
ENST00000542255.6:c.536+61C=
ENST00000543245.6:c.1748-29C=	ENSP00000438689.2:n.1748-29C=
ENST00000578319.5:n.260-29C=
ENST00000578711.1:n.1109C=
ENST00000578809.5:n.251-29C=
ENST00000579425.5:n.795-29C=
ENST00000579546.1:c.414-29C=
ENST00000582450.1:n.247C=
ENST00000583074.5:n.299+61C=
ENST00000583848.5:c.65-49C=	ENSP00000466487.1:n.65-49C=
ENST00000583850.5:n.450-29C=
ENST00000583858.5:c.610-29C=
ENST00000585203.6:n.870-29C=
NM_000018.3:c.1679-29C=	NP_000009.1:n.1679-29C=
NM_001033859.2:c.1613-29C=	NP_001029031.1:n.1613-29C=
NM_001270447.1:c.1748-29C=	NP_001257376.1:n.1748-29C=
NM_001270448.1:c.1451-29C=	NP_001257377.1:n.1451-29C=
XM_006721516.2:c.1678+61C=	XP_006721579.2:n.1678+61C=
XM_011523829.1:c.1576+61C=	XP_011522131.1:n.1576+61C=
XM_011523830.1:c.1577-29C=	XP_011522132.1:n.1577-29C=
XR_934021.1:n.1782-29C=
XR_934022.1:n.1688-29C=
XR_934023.1:n.1687+61C=
XM_006721516.3:c.1678+61C=	XP_006721579.2:n.1678+61C=
XM_011523829.2:c.1576+61C=	XP_011522131.1:n.1576+61C=
XM_011523830.2:c.1577-29C=	XP_011522132.1:n.1577-29C=
XM_024450741.1:c.1667-29C=	XP_024306509.1:n.1667-29C=
XR_934021.2:n.1734-29C=
XR_934022.2:n.1640-29C=
XR_934023.2:n.1639+61C=
NM_000018.4:c.1679-29C= MANE Select	NP_000009.1:n.1679-29C=
NM_001033859.3:c.1613-29C=	NP_001029031.1:n.1613-29C=
NM_001270447.2:c.1748-29C=	NP_001257376.1:n.1748-29C=
NM_001270448.2:c.1451-29C=	NP_001257377.1:n.1451-29C=