Canonical Allele Identifier: CA1028968897

Gene: SRD5A2

Linked Data

• gnomAD v3: 2-31567441-T-TGA
• gnomAD v4: 2-31567441-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567442_31567443insAG , CM000664.2:g.31567442_31567443insAG	GRCh38
NC_000002.11:g.31792512_31792513insAG , CM000664.1:g.31792512_31792513insAG	GRCh37
NC_000002.10:g.31646016_31646017insAG	NCBI36
NG_008365.1:g.18530_18531insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13178_281+13179insTC MANE Select	ENSP00000477587.1:n.281+13178_281+13179insTC
ENST00000622030.1:c.281+13178_281+13179insTC	ENSP00000477587.1:n.281+13178_281+13179insTC
NM_000348.3:c.281+13178_281+13179insTC	NP_000339.2:n.281+13178_281+13179insTC
XM_011533068.1:c.281+13178_281+13179insTC	XP_011531370.1:n.281+13178_281+13179insTC
XM_011533070.1:c.27-33676_27-33675insTC	XP_011531372.1:n.27-33676_27-33675insTC
XM_011533071.1:c.27-33676_27-33675insTC	XP_011531373.1:n.27-33676_27-33675insTC
XM_011533072.1:c.27-33676_27-33675insTC	XP_011531374.1:n.27-33676_27-33675insTC
XM_011533072.2:c.27-33676_27-33675insTC	XP_011531374.1:n.27-33676_27-33675insTC
NM_000348.4:c.281+13178_281+13179insTC MANE Select	NP_000339.2:n.281+13178_281+13179insTC