Canonical Allele Identifier: CA1242220999

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31580604_31580606delinsAAG , CM000664.2:g.31580604_31580606delinsAAG	GRCh38
NC_000002.11:g.31805674_31805676delinsAAG , CM000664.1:g.31805674_31805676delinsAAG	GRCh37
NC_000002.10:g.31659178_31659180delinsAAG	NCBI36
NG_008365.1:g.5366_5368delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+14_281+16delinsCTT MANE Select	ENSP00000477587.1:n.281+14_281+16delinsCTT
ENST00000622030.1:c.281+14_281+16delinsCTT	ENSP00000477587.1:n.281+14_281+16delinsCTT
NM_000348.3:c.281+14_281+16delinsCTT	NP_000339.2:n.281+14_281+16delinsCTT
XM_011533068.1:c.281+14_281+16delinsCTT	XP_011531370.1:n.281+14_281+16delinsCTT
XM_011533070.1:c.27-46840_27-46838delinsCTT	XP_011531372.1:n.27-46840_27-46838delinsCTT
XM_011533071.1:c.27-46840_27-46838delinsCTT	XP_011531373.1:n.27-46840_27-46838delinsCTT
XM_011533072.1:c.27-46840_27-46838delinsCTT	XP_011531374.1:n.27-46840_27-46838delinsCTT
XM_011533072.2:c.27-46840_27-46838delinsCTT	XP_011531374.1:n.27-46840_27-46838delinsCTT
NM_000348.4:c.281+14_281+16delinsCTT MANE Select	NP_000339.2:n.281+14_281+16delinsCTT