Canonical Allele Identifier: CA346598729

Gene: SRD5A2

Linked Data

• COSMIC: COSN26856926
• MyVariant Identifiers: chr2:g.31758832A>T (hg19) ; chr2:g.31533762A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533762A>T , CM000664.2:g.31533762A>T	GRCh38
NC_000002.11:g.31758832A>T , CM000664.1:g.31758832A>T	GRCh37
NC_000002.10:g.31612336A>T	NCBI36
NG_008365.1:g.52210T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.286T>A MANE Select	ENSP00000477587.1:p.Phe96Ile
ENST00000622030.1:c.286T>A	ENSP00000477587.1:p.Phe96Ile
NM_000348.3:c.286T>A	NP_000339.2:p.Phe96Ile
XM_011533068.1:c.286T>A	XP_011531370.1:p.Phe96Ile
XM_011533069.1:c.64T>A	XP_011531371.1:p.Phe22Ile
XM_011533070.1:c.31T>A	XP_011531372.1:p.Phe11Ile
XM_011533071.1:c.31T>A	XP_011531373.1:p.Phe11Ile
XM_011533072.1:c.31T>A	XP_011531374.1:p.Phe11Ile
XM_011533069.2:c.64T>A	XP_011531371.1:p.Phe22Ile
XM_011533072.2:c.31T>A	XP_011531374.1:p.Phe11Ile
NM_000348.4:c.286T>A MANE Select	NP_000339.2:p.Phe96Ile