Canonical Allele Identifier: CA1242220785

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31580304_31580306delinsCCT , CM000664.2:g.31580304_31580306delinsCCT	GRCh38
NC_000002.11:g.31805374_31805376delinsCCT , CM000664.1:g.31805374_31805376delinsCCT	GRCh37
NC_000002.10:g.31658878_31658880delinsCCT	NCBI36
NG_008365.1:g.5666_5668delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+314_281+316delinsAGG MANE Select	ENSP00000477587.1:n.281+314_281+316delinsAGG
ENST00000622030.1:c.281+314_281+316delinsAGG	ENSP00000477587.1:n.281+314_281+316delinsAGG
NM_000348.3:c.281+314_281+316delinsAGG	NP_000339.2:n.281+314_281+316delinsAGG
XM_011533068.1:c.281+314_281+316delinsAGG	XP_011531370.1:n.281+314_281+316delinsAGG
XM_011533070.1:c.27-46540_27-46538delinsAGG	XP_011531372.1:n.27-46540_27-46538delinsAGG
XM_011533071.1:c.27-46540_27-46538delinsAGG	XP_011531373.1:n.27-46540_27-46538delinsAGG
XM_011533072.1:c.27-46540_27-46538delinsAGG	XP_011531374.1:n.27-46540_27-46538delinsAGG
XM_011533072.2:c.27-46540_27-46538delinsAGG	XP_011531374.1:n.27-46540_27-46538delinsAGG
NM_000348.4:c.281+314_281+316delinsAGG MANE Select	NP_000339.2:n.281+314_281+316delinsAGG