Canonical Allele Identifier: CA2245701356
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222221_7222225delinsCAGTT , CM000679.2:g.7222221_7222225delinsCAGTT GRCh38
NC_000017.10:g.7125540_7125544delinsCAGTT , CM000679.1:g.7125540_7125544delinsCAGTT GRCh37
NC_000017.9:g.7066264_7066268delinsCAGTT NCBI36
NG_007975.1:g.7388_7392delinsCAGTT
NG_008391.2:g.2826_2830delinsAACTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.797_801delinsCAGTT MANE Select ENSP00000349297.5:p.Pro266=
ENST00000322910.9:c.*752_*756delinsCAGTT ENSP00000325395.5:n.*752_*756delinsCAGTT
ENST00000350303.9:c.731_735delinsCAGTT ENSP00000344152.5:p.Pro244=
ENST00000356839.9:c.797_801delinsCAGTT ENSP00000349297.5:p.Pro266=
ENST00000543245.6:c.866_870delinsCAGTT ENSP00000438689.2:p.Pro289=
ENST00000577191.5:n.969_973delinsCAGTT
ENST00000581378.5:c.515_519delinsCAGTT
ENST00000582379.1:n.181_185delinsCAGTT
NM_000018.3:c.797_801delinsCAGTT NP_000009.1:p.Pro266=
NM_001033859.2:c.731_735delinsCAGTT NP_001029031.1:p.Pro244=
NM_001270447.1:c.866_870delinsCAGTT NP_001257376.1:p.Pro289=
NM_001270448.1:c.569_573delinsCAGTT NP_001257377.1:p.Pro190=
XM_006721516.2:c.797_801delinsCAGTT XP_006721579.2:p.Pro266=
XM_011523829.1:c.797_801delinsCAGTT XP_011522131.1:p.Pro266=
XM_011523830.1:c.797_801delinsCAGTT XP_011522132.1:p.Pro266=
XR_934021.1:n.904_908delinsCAGTT
XR_934022.1:n.904_908delinsCAGTT
XR_934023.1:n.904_908delinsCAGTT
XM_006721516.3:c.797_801delinsCAGTT XP_006721579.2:p.Pro266=
XM_011523829.2:c.797_801delinsCAGTT XP_011522131.1:p.Pro266=
XM_011523830.2:c.797_801delinsCAGTT XP_011522132.1:p.Pro266=
XM_024450741.1:c.797_801delinsCAGTT XP_024306509.1:p.Pro266=
XR_934021.2:n.856_860delinsCAGTT
XR_934022.2:n.856_860delinsCAGTT
XR_934023.2:n.856_860delinsCAGTT
NM_000018.4:c.797_801delinsCAGTT MANE Select NP_000009.1:p.Pro266=
NM_001033859.3:c.731_735delinsCAGTT NP_001029031.1:p.Pro244=
NM_001270447.2:c.866_870delinsCAGTT NP_001257376.1:p.Pro289=
NM_001270448.2:c.569_573delinsCAGTT NP_001257377.1:p.Pro190=