Canonical Allele Identifier: CA375886134

Gene: AKR1C3 AKR1C2 AKR1C1

Linked Data

• MyVariant Identifiers: chr10:g.5141040T>A (hg19) ; chr10:g.5098848T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.5098848T>A , CM000672.2:g.5098848T>A	GRCh38
NC_000010.10:g.5141040T>A , CM000672.1:g.5141040T>A	GRCh37
NC_000010.9:g.5131040T>A	NCBI36
NG_047094.1:g.55083T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380554.5:c.416T>A (AKR1C3) MANE Select	ENSP00000369927.3:p.Phe139Tyr
ENST00000380554.4:c.416T>A (AKR1C3)	ENSP00000369927.3:p.Phe139Tyr
ENST00000407674.5:c.180+33826A>T (AKR1C2)	ENSP00000385221.2:n.180+33826A>T
ENST00000434459.6:c.933-8613T>A (AKR1C1)	ENSP00000412248.3:n.933-8613T>A
ENST00000439082.7:c.416T>A	ENSP00000401327.3:p.Phe139Tyr
ENST00000602997.5:c.347T>A (AKR1C3)	ENSP00000474188.1:p.Phe116Tyr
ENST00000605149.5:c.347T>A (AKR1C3)	ENSP00000474882.1:p.Phe116Tyr
ENST00000605322.1:n.280-479T>A (AKR1C3)
ENST00000605781.5:n.595T>A (AKR1C3)
NM_001253908.1:c.416T>A (AKR1C3)	NP_001240837.1:p.Phe139Tyr
NM_003739.5:c.416T>A (AKR1C3)	NP_003730.4:p.Phe139Tyr
NM_003739.6:c.416T>A (AKR1C3) MANE Select	NP_003730.4:p.Phe139Tyr
NM_001253908.2:c.416T>A (AKR1C3)	NP_001240837.1:p.Phe139Tyr