Canonical Allele Identifier: CA467990798

Linked Data

gnomAD v4: 10-5098867-T-C
MyVariant Identifiers: chr10:g.5141059T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098867T>C , CM000672.2:g.5098867T>C GRCh38
NC_000010.10:g.5141059T>C , CM000672.1:g.5141059T>C GRCh37
NC_000010.9:g.5131059T>C NCBI36
NG_047094.1:g.55102T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.435T>C (AKR1C3) MANE Select ENSP00000369927.3:p.Cys145=
ENST00000380554.4:c.435T>C (AKR1C3) ENSP00000369927.3:p.Cys145=
ENST00000407674.5:c.180+33807A>G (AKR1C2) ENSP00000385221.2:n.180+33807A>G
ENST00000434459.6:c.933-8594T>C (AKR1C1) ENSP00000412248.3:n.933-8594T>C
ENST00000439082.7:c.435T>C ENSP00000401327.3:p.Cys145=
ENST00000602997.5:c.366T>C (AKR1C3) ENSP00000474188.1:p.Cys122=
ENST00000605149.5:c.366T>C (AKR1C3) ENSP00000474882.1:p.Cys122=
ENST00000605322.1:n.280-460T>C (AKR1C3)
ENST00000605781.5:n.614T>C (AKR1C3)
NM_001253908.1:c.435T>C (AKR1C3) NP_001240837.1:p.Cys145=
NM_003739.5:c.435T>C (AKR1C3) NP_003730.4:p.Cys145=
NM_003739.6:c.435T>C (AKR1C3) MANE Select NP_003730.4:p.Cys145=
NM_001253908.2:c.435T>C (AKR1C3) NP_001240837.1:p.Cys145=