Canonical Allele Identifier: CA646614241

Gene: SRD5A2

Linked Data

• COSMIC: COSN14676315

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31568348_31568349insT , CM000664.2:g.31568348_31568349insT	GRCh38
NC_000002.11:g.31793418_31793419insT , CM000664.1:g.31793418_31793419insT	GRCh37
NC_000002.10:g.31646922_31646923insT	NCBI36
NG_008365.1:g.17623_17624insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+12271_281+12272insA MANE Select	ENSP00000477587.1:n.281+12271_281+12272insA
ENST00000622030.1:c.281+12271_281+12272insA	ENSP00000477587.1:n.281+12271_281+12272insA
NM_000348.3:c.281+12271_281+12272insA	NP_000339.2:n.281+12271_281+12272insA
XM_011533068.1:c.281+12271_281+12272insA	XP_011531370.1:n.281+12271_281+12272insA
XM_011533070.1:c.27-34583_27-34582insA	XP_011531372.1:n.27-34583_27-34582insA
XM_011533071.1:c.27-34583_27-34582insA	XP_011531373.1:n.27-34583_27-34582insA
XM_011533072.1:c.27-34583_27-34582insA	XP_011531374.1:n.27-34583_27-34582insA
XM_011533072.2:c.27-34583_27-34582insA	XP_011531374.1:n.27-34583_27-34582insA
NM_000348.4:c.281+12271_281+12272insA MANE Select	NP_000339.2:n.281+12271_281+12272insA