Canonical Allele Identifier: CA2245708851
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222537_7222538delinsTG , CM000679.2:g.7222537_7222538delinsTG GRCh38
NC_000017.10:g.7125856_7125857delinsTG , CM000679.1:g.7125856_7125857delinsTG GRCh37
NC_000017.9:g.7066580_7066581delinsTG NCBI36
NG_007975.1:g.7704_7705delinsTG
NG_008391.2:g.2513_2514delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.879-130_879-129delinsTG MANE Select ENSP00000349297.5:n.879-130_879-129delinsTG
ENST00000322910.9:c.*834-130_*834-129delinsTG ENSP00000325395.5:n.*834-130_*834-129delinsTG
ENST00000350303.9:c.813-130_813-129delinsTG ENSP00000344152.5:n.813-130_813-129delinsTG
ENST00000356839.9:c.879-130_879-129delinsTG ENSP00000349297.5:n.879-130_879-129delinsTG
ENST00000543245.6:c.948-130_948-129delinsTG ENSP00000438689.2:n.948-130_948-129delinsTG
ENST00000581378.5:c.597-130_597-129delinsTG
ENST00000582379.1:n.263-130_263-129delinsTG
NM_000018.3:c.879-130_879-129delinsTG NP_000009.1:n.879-130_879-129delinsTG
NM_001033859.2:c.813-130_813-129delinsTG NP_001029031.1:n.813-130_813-129delinsTG
NM_001270447.1:c.948-130_948-129delinsTG NP_001257376.1:n.948-130_948-129delinsTG
NM_001270448.1:c.651-130_651-129delinsTG NP_001257377.1:n.651-130_651-129delinsTG
XM_006721516.2:c.879-130_879-129delinsTG XP_006721579.2:n.879-130_879-129delinsTG
XM_011523829.1:c.879-130_879-129delinsTG XP_011522131.1:n.879-130_879-129delinsTG
XM_011523830.1:c.879-130_879-129delinsTG XP_011522132.1:n.879-130_879-129delinsTG
XR_934021.1:n.986-130_986-129delinsTG
XR_934022.1:n.986-130_986-129delinsTG
XR_934023.1:n.986-130_986-129delinsTG
XM_006721516.3:c.879-130_879-129delinsTG XP_006721579.2:n.879-130_879-129delinsTG
XM_011523829.2:c.879-130_879-129delinsTG XP_011522131.1:n.879-130_879-129delinsTG
XM_011523830.2:c.879-130_879-129delinsTG XP_011522132.1:n.879-130_879-129delinsTG
XM_024450741.1:c.879-130_879-129delinsTG XP_024306509.1:n.879-130_879-129delinsTG
XR_934021.2:n.938-130_938-129delinsTG
XR_934022.2:n.938-130_938-129delinsTG
XR_934023.2:n.938-130_938-129delinsTG
NM_000018.4:c.879-130_879-129delinsTG MANE Select NP_000009.1:n.879-130_879-129delinsTG
NM_001033859.3:c.813-130_813-129delinsTG NP_001029031.1:n.813-130_813-129delinsTG
NM_001270447.2:c.948-130_948-129delinsTG NP_001257376.1:n.948-130_948-129delinsTG
NM_001270448.2:c.651-130_651-129delinsTG NP_001257377.1:n.651-130_651-129delinsTG