Canonical Allele Identifier: CA924456429

Linked Data

dbSNP Id: rs1839283991

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5099031_5099032del , CM000672.2:g.5099031_5099032del GRCh38
NC_000010.10:g.5141223_5141224del , CM000672.1:g.5141223_5141224del GRCh37
NC_000010.9:g.5131223_5131224del NCBI36
NG_047094.1:g.55266_55267del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+152_447+153del (AKR1C3) MANE Select ENSP00000369927.3:n.447+152_447+153del
ENST00000380554.4:c.447+152_447+153del (AKR1C3) ENSP00000369927.3:n.447+152_447+153del
ENST00000407674.5:c.180+33645_180+33646del (AKR1C2) ENSP00000385221.2:n.180+33645_180+33646del
ENST00000434459.6:c.933-8430_933-8429del (AKR1C1) ENSP00000412248.3:n.933-8430_933-8429del
ENST00000439082.7:c.447+152_447+153del ENSP00000401327.3:n.447+152_447+153del
ENST00000602997.5:c.378+152_378+153del (AKR1C3) ENSP00000474188.1:n.378+152_378+153del
ENST00000605149.5:c.378+152_378+153del (AKR1C3) ENSP00000474882.1:n.378+152_378+153del
ENST00000605322.1:n.280-296_280-295del (AKR1C3)
ENST00000605781.5:n.626+152_626+153del (AKR1C3)
NM_001253908.1:c.447+152_447+153del (AKR1C3) NP_001240837.1:n.447+152_447+153del
NM_003739.5:c.447+152_447+153del (AKR1C3) NP_003730.4:n.447+152_447+153del
NM_003739.6:c.447+152_447+153del (AKR1C3) MANE Select NP_003730.4:n.447+152_447+153del
NM_001253908.2:c.447+152_447+153del (AKR1C3) NP_001240837.1:n.447+152_447+153del