Canonical Allele Identifier: CA591407975

Linked Data

dbSNP Id: rs1564369700

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098761_5098765del , CM000672.2:g.5098761_5098765del GRCh38
NC_000010.10:g.5140953_5140957del , CM000672.1:g.5140953_5140957del GRCh37
NC_000010.9:g.5130953_5130957del NCBI36
NG_047094.1:g.54996_55000del

Transcript Alleles

HGVS Amino-acid change
ENST00000380554.5:c.370-41_370-37del (AKR1C3) MANE Select ENSP00000369927.3:n.370-41_370-37del
ENST00000380554.4:c.370-41_370-37del (AKR1C3) ENSP00000369927.3:n.370-41_370-37del
ENST00000407674.5:c.180+33911_180+33915del (AKR1C2) ENSP00000385221.2:n.180+33911_180+33915del
ENST00000434459.6:c.933-8700_933-8696del (AKR1C1) ENSP00000412248.3:n.933-8700_933-8696del
ENST00000439082.7:c.370-41_370-37del ENSP00000401327.3:n.370-41_370-37del
ENST00000602997.5:c.301-41_301-37del (AKR1C3) ENSP00000474188.1:n.301-41_301-37del
ENST00000605149.5:c.301-41_301-37del (AKR1C3) ENSP00000474882.1:n.301-41_301-37del
ENST00000605322.1:n.280-566_280-562del (AKR1C3)
ENST00000605781.5:n.549-41_549-37del (AKR1C3)
NM_001253908.1:c.370-41_370-37del (AKR1C3) NP_001240837.1:n.370-41_370-37del
NM_003739.5:c.370-41_370-37del (AKR1C3) NP_003730.4:n.370-41_370-37del
NM_003739.6:c.370-41_370-37del (AKR1C3) MANE Select NP_003730.4:n.370-41_370-37del
NM_001253908.2:c.370-41_370-37del (AKR1C3) NP_001240837.1:n.370-41_370-37del