Canonical Allele Identifier: CA666181416
Gene: AKR1C3 HGNC NCBI
AKR1C2 HGNC NCBI
AKR1C1 HGNC NCBI

Linked Data

dbSNP Id: rs1271650729
gnomAD v4: 10-5098985-TCAGAAACTTTA-T
MyVariant Identifiers: chr10:g.5098986_5098996del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098988_5098998del , CM000672.2:g.5098988_5098998del GRCh38
NC_000010.10:g.5141180_5141190del , CM000672.1:g.5141180_5141190del GRCh37
NC_000010.9:g.5131180_5131190del NCBI36
NG_047094.1:g.55223_55233del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+109_447+119del (AKR1C3) MANE Select ENSP00000369927.3:n.447+109_447+119del
ENST00000380554.4:c.447+109_447+119del (AKR1C3) ENSP00000369927.3:n.447+109_447+119del
ENST00000407674.5:c.180+33678_180+33688del (AKR1C2) ENSP00000385221.2:n.180+33678_180+33688del
ENST00000434459.6:c.933-8473_933-8463del (AKR1C1) ENSP00000412248.3:n.933-8473_933-8463del
ENST00000439082.7:c.447+109_447+119del ENSP00000401327.3:n.447+109_447+119del
ENST00000602997.5:c.378+109_378+119del (AKR1C3) ENSP00000474188.1:n.378+109_378+119del
ENST00000605149.5:c.378+109_378+119del (AKR1C3) ENSP00000474882.1:n.378+109_378+119del
ENST00000605322.1:n.280-339_280-329del (AKR1C3)
ENST00000605781.5:n.626+109_626+119del (AKR1C3)
NM_001253908.1:c.447+109_447+119del (AKR1C3) NP_001240837.1:n.447+109_447+119del
NM_003739.5:c.447+109_447+119del (AKR1C3) NP_003730.4:n.447+109_447+119del
NM_003739.6:c.447+109_447+119del (AKR1C3) MANE Select NP_003730.4:n.447+109_447+119del
NM_001253908.2:c.447+109_447+119del (AKR1C3) NP_001240837.1:n.447+109_447+119del
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