Canonical Allele Identifier: CA1887557926

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098860_5098862delinsATC , CM000672.2:g.5098860_5098862delinsATC GRCh38
NC_000010.10:g.5141052_5141054delinsATC , CM000672.1:g.5141052_5141054delinsATC GRCh37
NC_000010.9:g.5131052_5131054delinsATC NCBI36
NG_047094.1:g.55095_55097delinsATC

Transcript Alleles

HGVS Amino-acid change
ENST00000380554.5:c.428_430delinsATC (AKR1C3) MANE Select ENSP00000369927.3:p.Asp143=
ENST00000380554.4:c.428_430delinsATC (AKR1C3) ENSP00000369927.3:p.Asp143=
ENST00000407674.5:c.180+33812_180+33814delinsGAT (AKR1C2) ENSP00000385221.2:n.180+33812_180+33814delinsGAT
ENST00000434459.6:c.933-8601_933-8599delinsATC (AKR1C1) ENSP00000412248.3:n.933-8601_933-8599delinsATC
ENST00000439082.7:c.428_430delinsATC ENSP00000401327.3:p.Asp143=
ENST00000602997.5:c.359_361delinsATC (AKR1C3) ENSP00000474188.1:p.Asp120=
ENST00000605149.5:c.359_361delinsATC (AKR1C3) ENSP00000474882.1:p.Asp120=
ENST00000605322.1:n.280-467_280-465delinsATC (AKR1C3)
ENST00000605781.5:n.607_609delinsATC (AKR1C3)
NM_001253908.1:c.428_430delinsATC (AKR1C3) NP_001240837.1:p.Asp143=
NM_003739.5:c.428_430delinsATC (AKR1C3) NP_003730.4:p.Asp143=
NM_003739.6:c.428_430delinsATC (AKR1C3) MANE Select NP_003730.4:p.Asp143=
NM_001253908.2:c.428_430delinsATC (AKR1C3) NP_001240837.1:p.Asp143=