Canonical Allele Identifier: CA375886172

Gene: AKR1C3 AKR1C2 AKR1C1

Linked Data

• gnomAD v4: 10-5098866-G-T
• MyVariant Identifiers: chr10:g.5141058G>T (hg19) ; chr10:g.5098866G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.5098866G>T , CM000672.2:g.5098866G>T	GRCh38
NC_000010.10:g.5141058G>T , CM000672.1:g.5141058G>T	GRCh37
NC_000010.9:g.5131058G>T	NCBI36
NG_047094.1:g.55101G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380554.5:c.434G>T (AKR1C3) MANE Select	ENSP00000369927.3:p.Cys145Phe
ENST00000380554.4:c.434G>T (AKR1C3)	ENSP00000369927.3:p.Cys145Phe
ENST00000407674.5:c.180+33808C>A (AKR1C2)	ENSP00000385221.2:n.180+33808C>A
ENST00000434459.6:c.933-8595G>T (AKR1C1)	ENSP00000412248.3:n.933-8595G>T
ENST00000439082.7:c.434G>T	ENSP00000401327.3:p.Cys145Phe
ENST00000602997.5:c.365G>T (AKR1C3)	ENSP00000474188.1:p.Cys122Phe
ENST00000605149.5:c.365G>T (AKR1C3)	ENSP00000474882.1:p.Cys122Phe
ENST00000605322.1:n.280-461G>T (AKR1C3)
ENST00000605781.5:n.613G>T (AKR1C3)
NM_001253908.1:c.434G>T (AKR1C3)	NP_001240837.1:p.Cys145Phe
NM_003739.5:c.434G>T (AKR1C3)	NP_003730.4:p.Cys145Phe
NM_003739.6:c.434G>T (AKR1C3) MANE Select	NP_003730.4:p.Cys145Phe
NM_001253908.2:c.434G>T (AKR1C3)	NP_001240837.1:p.Cys145Phe