Canonical Allele Identifier: CA346597801

Gene: SRD5A2

Linked Data

• COSMIC: COSN24408677
• MyVariant Identifiers: chr2:g.31751320C>G (hg19) ; chr2:g.31526250C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526250C>G , CM000664.2:g.31526250C>G	GRCh38
NC_000002.11:g.31751320C>G , CM000664.1:g.31751320C>G	GRCh37
NC_000002.10:g.31604824C>G	NCBI36
NG_008365.1:g.59722G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.711G>C MANE Select	ENSP00000477587.1:p.Lys237Asn
ENST00000622030.1:c.711G>C	ENSP00000477587.1:p.Lys237Asn
NM_000348.3:c.711G>C	NP_000339.2:p.Lys237Asn
XM_011533069.1:c.489G>C	XP_011531371.1:p.Lys163Asn
XM_011533070.1:c.456G>C	XP_011531372.1:p.Lys152Asn
XM_011533071.1:c.456G>C	XP_011531373.1:p.Lys152Asn
XM_011533072.1:c.456G>C	XP_011531374.1:p.Lys152Asn
XM_011533069.2:c.489G>C	XP_011531371.1:p.Lys163Asn
XM_011533072.2:c.456G>C	XP_011531374.1:p.Lys152Asn
NM_000348.4:c.711G>C MANE Select	NP_000339.2:p.Lys237Asn