Canonical Allele Identifier: CA591408194

Linked Data

dbSNP Id: rs1554785554
gnomAD v2: 10-5141083-G-T
MyVariant Identifiers: chr10:g.5141083G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098891G>T , CM000672.2:g.5098891G>T GRCh38
NC_000010.10:g.5141083G>T , CM000672.1:g.5141083G>T GRCh37
NC_000010.9:g.5131083G>T NCBI36
NG_047094.1:g.55126G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+12G>T (AKR1C3) MANE Select ENSP00000369927.3:n.447+12G>T
ENST00000380554.4:c.447+12G>T (AKR1C3) ENSP00000369927.3:n.447+12G>T
ENST00000407674.5:c.180+33783C>A (AKR1C2) ENSP00000385221.2:n.180+33783C>A
ENST00000434459.6:c.933-8570G>T (AKR1C1) ENSP00000412248.3:n.933-8570G>T
ENST00000439082.7:c.447+12G>T ENSP00000401327.3:n.447+12G>T
ENST00000602997.5:c.378+12G>T (AKR1C3) ENSP00000474188.1:n.378+12G>T
ENST00000605149.5:c.378+12G>T (AKR1C3) ENSP00000474882.1:n.378+12G>T
ENST00000605322.1:n.280-436G>T (AKR1C3)
ENST00000605781.5:n.626+12G>T (AKR1C3)
NM_001253908.1:c.447+12G>T (AKR1C3) NP_001240837.1:n.447+12G>T
NM_003739.5:c.447+12G>T (AKR1C3) NP_003730.4:n.447+12G>T
NM_003739.6:c.447+12G>T (AKR1C3) MANE Select NP_003730.4:n.447+12G>T
NM_001253908.2:c.447+12G>T (AKR1C3) NP_001240837.1:n.447+12G>T