Canonical Allele Identifier: CA767779362

Gene: SRD5A2

Linked Data

• MyVariant Identifiers: chr2:g.31792527_31792528insTA (hg19) ; chr2:g.31567457_31567458insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567457_31567458insTA , CM000664.2:g.31567457_31567458insTA	GRCh38
NC_000002.11:g.31792527_31792528insTA , CM000664.1:g.31792527_31792528insTA	GRCh37
NC_000002.10:g.31646031_31646032insTA	NCBI36
NG_008365.1:g.18514_18515insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13162_281+13163insTA MANE Select	ENSP00000477587.1:n.281+13162_281+13163insTA
ENST00000622030.1:c.281+13162_281+13163insTA	ENSP00000477587.1:n.281+13162_281+13163insTA
NM_000348.3:c.281+13162_281+13163insTA	NP_000339.2:n.281+13162_281+13163insTA
XM_011533068.1:c.281+13162_281+13163insTA	XP_011531370.1:n.281+13162_281+13163insTA
XM_011533070.1:c.27-33692_27-33691insTA	XP_011531372.1:n.27-33692_27-33691insTA
XM_011533071.1:c.27-33692_27-33691insTA	XP_011531373.1:n.27-33692_27-33691insTA
XM_011533072.1:c.27-33692_27-33691insTA	XP_011531374.1:n.27-33692_27-33691insTA
XM_011533072.2:c.27-33692_27-33691insTA	XP_011531374.1:n.27-33692_27-33691insTA
NM_000348.4:c.281+13162_281+13163insTA MANE Select	NP_000339.2:n.281+13162_281+13163insTA