Canonical Allele Identifier: CA2245713093

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224128G= , CM000679.2:g.7224128G=	GRCh38
NC_000017.10:g.7127447G= , CM000679.1:g.7127447G=	GRCh37
NC_000017.9:g.7068171G=	NCBI36
NG_007975.1:g.9295G=
NG_008391.2:g.923C=
NG_033038.1:g.15417C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1435-18G= MANE Select	ENSP00000349297.5:n.1435-18G=
ENST00000322910.9:c.*1390-18G=	ENSP00000325395.5:n.*1390-18G=
ENST00000350303.9:c.1369-18G=	ENSP00000344152.5:n.1369-18G=
ENST00000356839.9:c.1435-18G=	ENSP00000349297.5:n.1435-18G=
ENST00000542255.6:c.293-18G=
ENST00000543245.6:c.1504-18G=	ENSP00000438689.2:n.1504-18G=
ENST00000578711.1:n.624G=
ENST00000579391.1:n.25G=
ENST00000579425.5:n.551-18G=
ENST00000579546.1:c.271+59G=
ENST00000579894.5:n.204G=
ENST00000583074.5:n.153+59G=
ENST00000583850.5:n.210-18G=
ENST00000583858.5:c.463+59G=
ENST00000585203.6:n.626-18G=
NM_000018.3:c.1435-18G=	NP_000009.1:n.1435-18G=
NM_001033859.2:c.1369-18G=	NP_001029031.1:n.1369-18G=
NM_001270447.1:c.1504-18G=	NP_001257376.1:n.1504-18G=
NM_001270448.1:c.1207-18G=	NP_001257377.1:n.1207-18G=
XM_006721516.2:c.1435-18G=	XP_006721579.2:n.1435-18G=
XM_011523829.1:c.1434+59G=	XP_011522131.1:n.1434+59G=
XM_011523830.1:c.1434+59G=	XP_011522132.1:n.1434+59G=
XR_934021.1:n.1542-18G=
XR_934022.1:n.1541+59G=
XR_934023.1:n.1541+59G=
XM_006721516.3:c.1435-18G=	XP_006721579.2:n.1435-18G=
XM_011523829.2:c.1434+59G=	XP_011522131.1:n.1434+59G=
XM_011523830.2:c.1434+59G=	XP_011522132.1:n.1434+59G=
XM_024450741.1:c.1434+59G=	XP_024306509.1:n.1434+59G=
XR_934021.2:n.1494-18G=
XR_934022.2:n.1493+59G=
XR_934023.2:n.1493+59G=
NM_000018.4:c.1435-18G= MANE Select	NP_000009.1:n.1435-18G=
NM_001033859.3:c.1369-18G=	NP_001029031.1:n.1369-18G=
NM_001270447.2:c.1504-18G=	NP_001257376.1:n.1504-18G=
NM_001270448.2:c.1207-18G=	NP_001257377.1:n.1207-18G=