Canonical Allele Identifier: CA2841827529

Gene: ACADVL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7223112dup , CM000679.2:g.7223112dup	GRCh38
NC_000017.10:g.7126431dup , CM000679.1:g.7126431dup	GRCh37
NC_000017.9:g.7067155dup	NCBI36
NG_007975.1:g.8279dup
NG_008391.2:g.1941dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.1078-21dup MANE Select	ENSP00000349297.5:n.1078-21dup
ENST00000322910.9:c.*1033-21dup	ENSP00000325395.5:n.*1033-21dup
ENST00000350303.9:c.1012-21dup	ENSP00000344152.5:n.1012-21dup
ENST00000356839.9:c.1078-21dup	ENSP00000349297.5:n.1078-21dup
ENST00000543245.6:c.1147-21dup	ENSP00000438689.2:n.1147-21dup
ENST00000578579.2:n.6dup
ENST00000578824.5:n.473dup
ENST00000579425.5:n.81dup
ENST00000582379.1:n.708dup
ENST00000583858.5:c.107-21dup
ENST00000585203.6:n.265dup
NM_000018.3:c.1078-21dup	NP_000009.1:n.1078-21dup
NM_001033859.2:c.1012-21dup	NP_001029031.1:n.1012-21dup
NM_001270447.1:c.1147-21dup	NP_001257376.1:n.1147-21dup
NM_001270448.1:c.850-21dup	NP_001257377.1:n.850-21dup
XM_006721516.2:c.1078-21dup	XP_006721579.2:n.1078-21dup
XM_011523829.1:c.1078-21dup	XP_011522131.1:n.1078-21dup
XM_011523830.1:c.1078-21dup	XP_011522132.1:n.1078-21dup
XR_934021.1:n.1185-21dup
XR_934022.1:n.1185-21dup
XR_934023.1:n.1185-21dup
XM_006721516.3:c.1078-21dup	XP_006721579.2:n.1078-21dup
XM_011523829.2:c.1078-21dup	XP_011522131.1:n.1078-21dup
XM_011523830.2:c.1078-21dup	XP_011522132.1:n.1078-21dup
XM_024450741.1:c.1078-21dup	XP_024306509.1:n.1078-21dup
XR_934021.2:n.1137-21dup
XR_934022.2:n.1137-21dup
XR_934023.2:n.1137-21dup
NM_000018.4:c.1078-21dup MANE Select	NP_000009.1:n.1078-21dup
NM_001033859.3:c.1012-21dup	NP_001029031.1:n.1012-21dup
NM_001270447.2:c.1147-21dup	NP_001257376.1:n.1147-21dup
NM_001270448.2:c.850-21dup	NP_001257377.1:n.850-21dup