Canonical Allele Identifier: CA1887558023

Linked Data

dbSNP Id: rs1839283789
gnomAD v4: 10-5099015-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5099015G>A , CM000672.2:g.5099015G>A GRCh38
NC_000010.10:g.5141207G>A , CM000672.1:g.5141207G>A GRCh37
NC_000010.9:g.5131207G>A NCBI36
NG_047094.1:g.55250G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+136G>A (AKR1C3) MANE Select ENSP00000369927.3:n.447+136G>A
ENST00000380554.4:c.447+136G>A (AKR1C3) ENSP00000369927.3:n.447+136G>A
ENST00000407674.5:c.180+33659C>T (AKR1C2) ENSP00000385221.2:n.180+33659C>T
ENST00000434459.6:c.933-8446G>A (AKR1C1) ENSP00000412248.3:n.933-8446G>A
ENST00000439082.7:c.447+136G>A ENSP00000401327.3:n.447+136G>A
ENST00000602997.5:c.378+136G>A (AKR1C3) ENSP00000474188.1:n.378+136G>A
ENST00000605149.5:c.378+136G>A (AKR1C3) ENSP00000474882.1:n.378+136G>A
ENST00000605322.1:n.280-312G>A (AKR1C3)
ENST00000605781.5:n.626+136G>A (AKR1C3)
NM_001253908.1:c.447+136G>A (AKR1C3) NP_001240837.1:n.447+136G>A
NM_003739.5:c.447+136G>A (AKR1C3) NP_003730.4:n.447+136G>A
NM_003739.6:c.447+136G>A (AKR1C3) MANE Select NP_003730.4:n.447+136G>A
NM_001253908.2:c.447+136G>A (AKR1C3) NP_001240837.1:n.447+136G>A