Canonical Allele Identifier: CA2808366115
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7223492_7223493insG , CM000679.2:g.7223492_7223493insG GRCh38
NC_000017.10:g.7126811_7126812insG , CM000679.1:g.7126811_7126812insG GRCh37
NC_000017.9:g.7067535_7067536insG NCBI36
NG_007975.1:g.8659_8660insG
NG_008391.2:g.1558_1559insC
NG_033038.1:g.16052_16053insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1183-152_1183-151insG MANE Select ENSP00000349297.5:n.1183-152_1183-151insG
ENST00000322910.9:c.*1138-152_*1138-151insG ENSP00000325395.5:n.*1138-152_*1138-151insG
ENST00000350303.9:c.1117-152_1117-151insG ENSP00000344152.5:n.1117-152_1117-151insG
ENST00000356839.9:c.1183-152_1183-151insG ENSP00000349297.5:n.1183-152_1183-151insG
ENST00000542255.6:c.41-152_41-151insG
ENST00000543245.6:c.1252-152_1252-151insG ENSP00000438689.2:n.1252-152_1252-151insG
ENST00000578579.2:n.202_203insG
ENST00000578824.5:n.599-152_599-151insG
ENST00000579425.5:n.207-152_207-151insG
ENST00000579546.1:c.20-152_20-151insG
ENST00000583858.5:c.212-152_212-151insG
ENST00000585203.6:n.391-152_391-151insG
NM_000018.3:c.1183-152_1183-151insG NP_000009.1:n.1183-152_1183-151insG
NM_001033859.2:c.1117-152_1117-151insG NP_001029031.1:n.1117-152_1117-151insG
NM_001270447.1:c.1252-152_1252-151insG NP_001257376.1:n.1252-152_1252-151insG
NM_001270448.1:c.955-152_955-151insG NP_001257377.1:n.955-152_955-151insG
XM_006721516.2:c.1183-152_1183-151insG XP_006721579.2:n.1183-152_1183-151insG
XM_011523829.1:c.1183-152_1183-151insG XP_011522131.1:n.1183-152_1183-151insG
XM_011523830.1:c.1183-152_1183-151insG XP_011522132.1:n.1183-152_1183-151insG
XR_934021.1:n.1290-152_1290-151insG
XR_934022.1:n.1290-152_1290-151insG
XR_934023.1:n.1290-152_1290-151insG
XM_006721516.3:c.1183-152_1183-151insG XP_006721579.2:n.1183-152_1183-151insG
XM_011523829.2:c.1183-152_1183-151insG XP_011522131.1:n.1183-152_1183-151insG
XM_011523830.2:c.1183-152_1183-151insG XP_011522132.1:n.1183-152_1183-151insG
XM_024450741.1:c.1183-152_1183-151insG XP_024306509.1:n.1183-152_1183-151insG
XR_934021.2:n.1242-152_1242-151insG
XR_934022.2:n.1242-152_1242-151insG
XR_934023.2:n.1242-152_1242-151insG
NM_000018.4:c.1183-152_1183-151insG MANE Select NP_000009.1:n.1183-152_1183-151insG
NM_001033859.3:c.1117-152_1117-151insG NP_001029031.1:n.1117-152_1117-151insG
NM_001270447.2:c.1252-152_1252-151insG NP_001257376.1:n.1252-152_1252-151insG
NM_001270448.2:c.955-152_955-151insG NP_001257377.1:n.955-152_955-151insG