Canonical Allele Identifier: CA2245714097

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224405G= , CM000679.2:g.7224405G=	GRCh38
NC_000017.10:g.7127724G= , CM000679.1:g.7127724G=	GRCh37
NC_000017.9:g.7068448G=	NCBI36
NG_007975.1:g.9572G=
NG_008391.2:g.646C=
NG_033038.1:g.15140C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1605+12G= MANE Select	ENSP00000349297.5:n.1605+12G=
ENST00000322910.9:c.*1560+12G=	ENSP00000325395.5:n.*1560+12G=
ENST00000350303.9:c.1539+12G=	ENSP00000344152.5:n.1539+12G=
ENST00000356839.9:c.1605+12G=	ENSP00000349297.5:n.1605+12G=
ENST00000542255.6:c.463+12G=
ENST00000543245.6:c.1674+12G=	ENSP00000438689.2:n.1674+12G=
ENST00000578319.5:n.112G=
ENST00000578711.1:n.901G=
ENST00000578809.5:n.177+12G=
ENST00000579391.1:n.213+12G=
ENST00000579425.5:n.721+12G=
ENST00000579546.1:c.344+12G=
ENST00000579894.5:n.392+12G=
ENST00000582450.1:n.113+12G=
ENST00000583074.5:n.226+12G=
ENST00000583850.5:n.380+12G=
ENST00000583858.5:c.536+12G=
ENST00000585203.6:n.796+12G=
NM_000018.3:c.1605+12G=	NP_000009.1:n.1605+12G=
NM_001033859.2:c.1539+12G=	NP_001029031.1:n.1539+12G=
NM_001270447.1:c.1674+12G=	NP_001257376.1:n.1674+12G=
NM_001270448.1:c.1377+12G=	NP_001257377.1:n.1377+12G=
XM_006721516.2:c.1605+12G=	XP_006721579.2:n.1605+12G=
XM_011523829.1:c.1507+12G=	XP_011522131.1:n.1507+12G=
XM_011523830.1:c.1507+12G=	XP_011522132.1:n.1507+12G=
XR_934021.1:n.1712+12G=
XR_934022.1:n.1614+12G=
XR_934023.1:n.1614+12G=
XM_006721516.3:c.1605+12G=	XP_006721579.2:n.1605+12G=
XM_011523829.2:c.1507+12G=	XP_011522131.1:n.1507+12G=
XM_011523830.2:c.1507+12G=	XP_011522132.1:n.1507+12G=
XM_024450741.1:c.1519G=	XP_024306509.1:p.Gly507=
XR_934021.2:n.1664+12G=
XR_934022.2:n.1566+12G=
XR_934023.2:n.1566+12G=
NM_000018.4:c.1605+12G= MANE Select	NP_000009.1:n.1605+12G=
NM_001033859.3:c.1539+12G=	NP_001029031.1:n.1539+12G=
NM_001270447.2:c.1674+12G=	NP_001257376.1:n.1674+12G=
NM_001270448.2:c.1377+12G=	NP_001257377.1:n.1377+12G=