Canonical Allele Identifier: CA1242220746

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31580250_31580251delinsTA , CM000664.2:g.31580250_31580251delinsTA	GRCh38
NC_000002.11:g.31805320_31805321delinsTA , CM000664.1:g.31805320_31805321delinsTA	GRCh37
NC_000002.10:g.31658824_31658825delinsTA	NCBI36
NG_008365.1:g.5721_5722delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+369_281+370delinsTA MANE Select	ENSP00000477587.1:n.281+369_281+370delinsTA
ENST00000622030.1:c.281+369_281+370delinsTA	ENSP00000477587.1:n.281+369_281+370delinsTA
NM_000348.3:c.281+369_281+370delinsTA	NP_000339.2:n.281+369_281+370delinsTA
XM_011533068.1:c.281+369_281+370delinsTA	XP_011531370.1:n.281+369_281+370delinsTA
XM_011533070.1:c.27-46485_27-46484delinsTA	XP_011531372.1:n.27-46485_27-46484delinsTA
XM_011533071.1:c.27-46485_27-46484delinsTA	XP_011531373.1:n.27-46485_27-46484delinsTA
XM_011533072.1:c.27-46485_27-46484delinsTA	XP_011531374.1:n.27-46485_27-46484delinsTA
XM_011533072.2:c.27-46485_27-46484delinsTA	XP_011531374.1:n.27-46485_27-46484delinsTA
NM_000348.4:c.281+369_281+370delinsTA MANE Select	NP_000339.2:n.281+369_281+370delinsTA