Canonical Allele Identifier: CA924456367

Linked Data

dbSNP Id: rs1839281347

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098930_5098931insCTTCTC , CM000672.2:g.5098930_5098931insCTTCTC GRCh38
NC_000010.10:g.5141122_5141123insCTTCTC , CM000672.1:g.5141122_5141123insCTTCTC GRCh37
NC_000010.9:g.5131122_5131123insCTTCTC NCBI36
NG_047094.1:g.55165_55166insCTTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+51_447+52insCTTCTC (AKR1C3) MANE Select ENSP00000369927.3:n.447+51_447+52insCTTCTC
ENST00000380554.4:c.447+51_447+52insCTTCTC (AKR1C3) ENSP00000369927.3:n.447+51_447+52insCTTCTC
ENST00000407674.5:c.180+33745_180+33746insGAAGGA (AKR1C2) ENSP00000385221.2:n.180+33745_180+33746insGAAGGA
ENST00000434459.6:c.933-8531_933-8530insCTTCTC (AKR1C1) ENSP00000412248.3:n.933-8531_933-8530insCTTCTC
ENST00000439082.7:c.447+51_447+52insCTTCTC ENSP00000401327.3:n.447+51_447+52insCTTCTC
ENST00000602997.5:c.378+51_378+52insCTTCTC (AKR1C3) ENSP00000474188.1:n.378+51_378+52insCTTCTC
ENST00000605149.5:c.378+51_378+52insCTTCTC (AKR1C3) ENSP00000474882.1:n.378+51_378+52insCTTCTC
ENST00000605322.1:n.280-397_280-396insCTTCTC (AKR1C3)
ENST00000605781.5:n.626+51_626+52insCTTCTC (AKR1C3)
NM_001253908.1:c.447+51_447+52insCTTCTC (AKR1C3) NP_001240837.1:n.447+51_447+52insCTTCTC
NM_003739.5:c.447+51_447+52insCTTCTC (AKR1C3) NP_003730.4:n.447+51_447+52insCTTCTC
NM_003739.6:c.447+51_447+52insCTTCTC (AKR1C3) MANE Select NP_003730.4:n.447+51_447+52insCTTCTC
NM_001253908.2:c.447+51_447+52insCTTCTC (AKR1C3) NP_001240837.1:n.447+51_447+52insCTTCTC