Canonical Allele Identifier: CA1242214985

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31568167_31568169delinsAAG , CM000664.2:g.31568167_31568169delinsAAG	GRCh38
NC_000002.11:g.31793237_31793239delinsAAG , CM000664.1:g.31793237_31793239delinsAAG	GRCh37
NC_000002.10:g.31646741_31646743delinsAAG	NCBI36
NG_008365.1:g.17803_17805delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+12451_281+12453delinsCTT MANE Select	ENSP00000477587.1:n.281+12451_281+12453delinsCTT
ENST00000622030.1:c.281+12451_281+12453delinsCTT	ENSP00000477587.1:n.281+12451_281+12453delinsCTT
NM_000348.3:c.281+12451_281+12453delinsCTT	NP_000339.2:n.281+12451_281+12453delinsCTT
XM_011533068.1:c.281+12451_281+12453delinsCTT	XP_011531370.1:n.281+12451_281+12453delinsCTT
XM_011533070.1:c.27-34403_27-34401delinsCTT	XP_011531372.1:n.27-34403_27-34401delinsCTT
XM_011533071.1:c.27-34403_27-34401delinsCTT	XP_011531373.1:n.27-34403_27-34401delinsCTT
XM_011533072.1:c.27-34403_27-34401delinsCTT	XP_011531374.1:n.27-34403_27-34401delinsCTT
XM_011533072.2:c.27-34403_27-34401delinsCTT	XP_011531374.1:n.27-34403_27-34401delinsCTT
NM_000348.4:c.281+12451_281+12453delinsCTT MANE Select	NP_000339.2:n.281+12451_281+12453delinsCTT