Canonical Allele Identifier: CA2608080773

Gene: AKR1C3 AKR1C2 AKR1C1

Linked Data

• dbSNP Id: rs2131842529
• gnomAD v4: 10-5099020-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.5099020A>G , CM000672.2:g.5099020A>G	GRCh38
NC_000010.10:g.5141212A>G , CM000672.1:g.5141212A>G	GRCh37
NC_000010.9:g.5131212A>G	NCBI36
NG_047094.1:g.55255A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380554.5:c.447+141A>G (AKR1C3) MANE Select	ENSP00000369927.3:n.447+141A>G
ENST00000380554.4:c.447+141A>G (AKR1C3)	ENSP00000369927.3:n.447+141A>G
ENST00000407674.5:c.180+33654T>C (AKR1C2)	ENSP00000385221.2:n.180+33654T>C
ENST00000434459.6:c.933-8441A>G (AKR1C1)	ENSP00000412248.3:n.933-8441A>G
ENST00000439082.7:c.447+141A>G	ENSP00000401327.3:n.447+141A>G
ENST00000602997.5:c.378+141A>G (AKR1C3)	ENSP00000474188.1:n.378+141A>G
ENST00000605149.5:c.378+141A>G (AKR1C3)	ENSP00000474882.1:n.378+141A>G
ENST00000605322.1:n.280-307A>G (AKR1C3)
ENST00000605781.5:n.626+141A>G (AKR1C3)
NM_001253908.1:c.447+141A>G (AKR1C3)	NP_001240837.1:n.447+141A>G
NM_003739.5:c.447+141A>G (AKR1C3)	NP_003730.4:n.447+141A>G
NM_003739.6:c.447+141A>G (AKR1C3) MANE Select	NP_003730.4:n.447+141A>G
NM_001253908.2:c.447+141A>G (AKR1C3)	NP_001240837.1:n.447+141A>G