Canonical Allele Identifier: CA467990787

Gene: AKR1C3 AKR1C2 AKR1C1

Linked Data

• MyVariant Identifiers: chr10:g.5141041T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.5098849T>C , CM000672.2:g.5098849T>C	GRCh38
NC_000010.10:g.5141041T>C , CM000672.1:g.5141041T>C	GRCh37
NC_000010.9:g.5131041T>C	NCBI36
NG_047094.1:g.55084T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000380554.5:c.417T>C (AKR1C3) MANE Select	ENSP00000369927.3:p.Phe139=
ENST00000380554.4:c.417T>C (AKR1C3)	ENSP00000369927.3:p.Phe139=
ENST00000407674.5:c.180+33825A>G (AKR1C2)	ENSP00000385221.2:n.180+33825A>G
ENST00000434459.6:c.933-8612T>C (AKR1C1)	ENSP00000412248.3:n.933-8612T>C
ENST00000439082.7:c.417T>C	ENSP00000401327.3:p.Phe139=
ENST00000602997.5:c.348T>C (AKR1C3)	ENSP00000474188.1:p.Phe116=
ENST00000605149.5:c.348T>C (AKR1C3)	ENSP00000474882.1:p.Phe116=
ENST00000605322.1:n.280-478T>C (AKR1C3)
ENST00000605781.5:n.596T>C (AKR1C3)
NM_001253908.1:c.417T>C (AKR1C3)	NP_001240837.1:p.Phe139=
NM_003739.5:c.417T>C (AKR1C3)	NP_003730.4:p.Phe139=
NM_003739.6:c.417T>C (AKR1C3) MANE Select	NP_003730.4:p.Phe139=
NM_001253908.2:c.417T>C (AKR1C3)	NP_001240837.1:p.Phe139=