Canonical Allele Identifier: CA2245714679

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7224562C= , CM000679.2:g.7224562C=	GRCh38
NC_000017.10:g.7127881C= , CM000679.1:g.7127881C=	GRCh37
NC_000017.9:g.7068605C=	NCBI36
NG_007975.1:g.9729C=
NG_008391.2:g.489G=
NG_033038.1:g.14983G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1678+10C= MANE Select	ENSP00000349297.5:n.1678+10C=
ENST00000322910.9:c.*1633+10C=	ENSP00000325395.5:n.*1633+10C=
ENST00000350303.9:c.1612+10C=	ENSP00000344152.5:n.1612+10C=
ENST00000356839.9:c.1678+10C=	ENSP00000349297.5:n.1678+10C=
ENST00000542255.6:c.536+10C=
ENST00000543245.6:c.1747+10C=	ENSP00000438689.2:n.1747+10C=
ENST00000578319.5:n.259+10C=
ENST00000578711.1:n.1058C=
ENST00000578809.5:n.250+10C=
ENST00000579391.1:n.292C=
ENST00000579425.5:n.794+10C=
ENST00000579546.1:c.413+10C=
ENST00000582450.1:n.196C=
ENST00000583074.5:n.299+10C=
ENST00000583848.5:c.64+10C=	ENSP00000466487.1:n.64+10C=
ENST00000583850.5:n.449+10C=
ENST00000583858.5:c.609+10C=
ENST00000585203.6:n.869+10C=
NM_000018.3:c.1678+10C=	NP_000009.1:n.1678+10C=
NM_001033859.2:c.1612+10C=	NP_001029031.1:n.1612+10C=
NM_001270447.1:c.1747+10C=	NP_001257376.1:n.1747+10C=
NM_001270448.1:c.1450+10C=	NP_001257377.1:n.1450+10C=
XM_006721516.2:c.1678+10C=	XP_006721579.2:n.1678+10C=
XM_011523829.1:c.1576+10C=	XP_011522131.1:n.1576+10C=
XM_011523830.1:c.1576+10C=	XP_011522132.1:n.1576+10C=
XR_934021.1:n.1781+10C=
XR_934022.1:n.1687+10C=
XR_934023.1:n.1687+10C=
XM_006721516.3:c.1678+10C=	XP_006721579.2:n.1678+10C=
XM_011523829.2:c.1576+10C=	XP_011522131.1:n.1576+10C=
XM_011523830.2:c.1576+10C=	XP_011522132.1:n.1576+10C=
XM_024450741.1:c.1666+10C=	XP_024306509.1:n.1666+10C=
XR_934021.2:n.1733+10C=
XR_934022.2:n.1639+10C=
XR_934023.2:n.1639+10C=
NM_000018.4:c.1678+10C= MANE Select	NP_000009.1:n.1678+10C=
NM_001033859.3:c.1612+10C=	NP_001029031.1:n.1612+10C=
NM_001270447.2:c.1747+10C=	NP_001257376.1:n.1747+10C=
NM_001270448.2:c.1450+10C=	NP_001257377.1:n.1450+10C=