Canonical Allele Identifier: CA2245716668

Gene: ACADVL

Linked Data

• dbSNP Id: rs2071417278
• gnomAD v4: 17-7225105-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7225107dup , CM000679.2:g.7225107dup	GRCh38
NC_000017.10:g.7128426dup , CM000679.1:g.7128426dup	GRCh37
NC_000017.9:g.7069150dup	NCBI36
NG_007975.1:g.10274dup
NG_033038.1:g.14439dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356839.10:c.*10dup MANE Select	ENSP00000349297.5:n.*10dup
ENST00000322910.9:c.*1933dup	ENSP00000325395.5:n.*1933dup
ENST00000350303.9:c.*10dup	ENSP00000344152.5:n.*10dup
ENST00000356839.9:c.*10dup	ENSP00000349297.5:n.*10dup
ENST00000542255.6:c.857dup
ENST00000543245.6:c.*10dup	ENSP00000438689.2:n.*10dup
ENST00000578033.1:n.403dup
ENST00000578319.5:n.559dup
ENST00000578711.1:n.1603dup
ENST00000578809.5:n.550dup
ENST00000579425.5:n.1094dup
ENST00000583848.5:c.344dup	ENSP00000466487.1:n.344dup
ENST00000583850.5:n.749dup
ENST00000583858.5:c.909dup
NM_000018.3:c.*10dup	NP_000009.1:n.*10dup
NM_001033859.2:c.*10dup	NP_001029031.1:n.*10dup
NM_001270447.1:c.*10dup	NP_001257376.1:n.*10dup
NM_001270448.1:c.*10dup	NP_001257377.1:n.*10dup
XM_006721516.2:c.*10dup	XP_006721579.2:n.*10dup
XM_011523829.1:c.*10dup	XP_011522131.1:n.*10dup
XM_011523830.1:c.*10dup	XP_011522132.1:n.*10dup
XR_934021.1:n.2081dup
XR_934022.1:n.1987dup
XR_934023.1:n.2008dup
XM_006721516.3:c.*10dup	XP_006721579.2:n.*10dup
XM_011523829.2:c.*10dup	XP_011522131.1:n.*10dup
XM_011523830.2:c.*10dup	XP_011522132.1:n.*10dup
XM_024450741.1:c.*10dup	XP_024306509.1:n.*10dup
XR_934021.2:n.2033dup
XR_934022.2:n.1939dup
XR_934023.2:n.1960dup
NM_000018.4:c.*10dup MANE Select	NP_000009.1:n.*10dup
NM_001033859.3:c.*10dup	NP_001029031.1:n.*10dup
NM_001270447.2:c.*10dup	NP_001257376.1:n.*10dup
NM_001270448.2:c.*10dup	NP_001257377.1:n.*10dup