Canonical Allele Identifier: CA375886176

Gene: AKR1C3 AKR1C2 AKR1C1

Linked Data

• dbSNP Id: rs1554785553
• gnomAD v2: 10-5141060-A-G
• gnomAD v3: 10-5098868-A-G
• gnomAD v4: 10-5098868-A-G
• MyVariant Identifiers: chr10:g.5141060A>G (hg19) ; chr10:g.5098868A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.5098868A>G , CM000672.2:g.5098868A>G	GRCh38
NC_000010.10:g.5141060A>G , CM000672.1:g.5141060A>G	GRCh37
NC_000010.9:g.5131060A>G	NCBI36
NG_047094.1:g.55103A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380554.5:c.436A>G (AKR1C3) MANE Select	ENSP00000369927.3:p.Thr146Ala
ENST00000380554.4:c.436A>G (AKR1C3)	ENSP00000369927.3:p.Thr146Ala
ENST00000407674.5:c.180+33806T>C (AKR1C2)	ENSP00000385221.2:n.180+33806T>C
ENST00000434459.6:c.933-8593A>G (AKR1C1)	ENSP00000412248.3:n.933-8593A>G
ENST00000439082.7:c.436A>G	ENSP00000401327.3:p.Thr146Ala
ENST00000602997.5:c.367A>G (AKR1C3)	ENSP00000474188.1:p.Thr123Ala
ENST00000605149.5:c.367A>G (AKR1C3)	ENSP00000474882.1:p.Thr123Ala
ENST00000605322.1:n.280-459A>G (AKR1C3)
ENST00000605781.5:n.615A>G (AKR1C3)
NM_001253908.1:c.436A>G (AKR1C3)	NP_001240837.1:p.Thr146Ala
NM_003739.5:c.436A>G (AKR1C3)	NP_003730.4:p.Thr146Ala
NM_003739.6:c.436A>G (AKR1C3) MANE Select	NP_003730.4:p.Thr146Ala
NM_001253908.2:c.436A>G (AKR1C3)	NP_001240837.1:p.Thr146Ala