Canonical Allele Identifier: CA2839899638

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223087dup , CM000679.2:g.7223087dup	GRCh38
NC_000017.10:g.7126406dup , CM000679.1:g.7126406dup	GRCh37
NC_000017.9:g.7067130dup	NCBI36
NG_007975.1:g.8254dup
NG_008391.2:g.1964dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1078-46dup MANE Select	ENSP00000349297.5:n.1078-46dup
ENST00000322910.9:c.*1033-46dup	ENSP00000325395.5:n.*1033-46dup
ENST00000350303.9:c.1012-46dup	ENSP00000344152.5:n.1012-46dup
ENST00000356839.9:c.1078-46dup	ENSP00000349297.5:n.1078-46dup
ENST00000543245.6:c.1147-46dup	ENSP00000438689.2:n.1147-46dup
ENST00000578824.5:n.448dup
ENST00000579425.5:n.56dup
ENST00000582379.1:n.683dup
ENST00000583858.5:c.107-46dup
ENST00000585203.6:n.240dup
NM_000018.3:c.1078-46dup	NP_000009.1:n.1078-46dup
NM_001033859.2:c.1012-46dup	NP_001029031.1:n.1012-46dup
NM_001270447.1:c.1147-46dup	NP_001257376.1:n.1147-46dup
NM_001270448.1:c.850-46dup	NP_001257377.1:n.850-46dup
XM_006721516.2:c.1078-46dup	XP_006721579.2:n.1078-46dup
XM_011523829.1:c.1078-46dup	XP_011522131.1:n.1078-46dup
XM_011523830.1:c.1078-46dup	XP_011522132.1:n.1078-46dup
XR_934021.1:n.1185-46dup
XR_934022.1:n.1185-46dup
XR_934023.1:n.1185-46dup
XM_006721516.3:c.1078-46dup	XP_006721579.2:n.1078-46dup
XM_011523829.2:c.1078-46dup	XP_011522131.1:n.1078-46dup
XM_011523830.2:c.1078-46dup	XP_011522132.1:n.1078-46dup
XM_024450741.1:c.1078-46dup	XP_024306509.1:n.1078-46dup
XR_934021.2:n.1137-46dup
XR_934022.2:n.1137-46dup
XR_934023.2:n.1137-46dup
NM_000018.4:c.1078-46dup MANE Select	NP_000009.1:n.1078-46dup
NM_001033859.3:c.1012-46dup	NP_001029031.1:n.1012-46dup
NM_001270447.2:c.1147-46dup	NP_001257376.1:n.1147-46dup
NM_001270448.2:c.850-46dup	NP_001257377.1:n.850-46dup