Canonical Allele Identifier: CA1242197359

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529301_31529302delinsAT , CM000664.2:g.31529301_31529302delinsAT	GRCh38
NC_000002.11:g.31754371_31754372delinsAT , CM000664.1:g.31754371_31754372delinsAT	GRCh37
NC_000002.10:g.31607875_31607876delinsAT	NCBI36
NG_008365.1:g.56670_56671delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.698+5_698+6delinsAT MANE Select	ENSP00000477587.1:n.698+5_698+6delinsAT
ENST00000622030.1:c.698+5_698+6delinsAT	ENSP00000477587.1:n.698+5_698+6delinsAT
NM_000348.3:c.698+5_698+6delinsAT	NP_000339.2:n.698+5_698+6delinsAT
XM_011533069.1:c.476+5_476+6delinsAT	XP_011531371.1:n.476+5_476+6delinsAT
XM_011533070.1:c.443+5_443+6delinsAT	XP_011531372.1:n.443+5_443+6delinsAT
XM_011533071.1:c.443+5_443+6delinsAT	XP_011531373.1:n.443+5_443+6delinsAT
XM_011533072.1:c.443+5_443+6delinsAT	XP_011531374.1:n.443+5_443+6delinsAT
XM_011533069.2:c.476+5_476+6delinsAT	XP_011531371.1:n.476+5_476+6delinsAT
XM_011533072.2:c.443+5_443+6delinsAT	XP_011531374.1:n.443+5_443+6delinsAT
NM_000348.4:c.698+5_698+6delinsAT MANE Select	NP_000339.2:n.698+5_698+6delinsAT