Canonical Allele Identifier: CA5669647
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs772358415

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837246_102837255del , CM000672.2:g.102837246_102837255del GRCh38
NC_000010.10:g.104597003_104597012del , CM000672.1:g.104597003_104597012del GRCh37
NC_000010.9:g.104586993_104587002del NCBI36
NG_007955.1:g.5279_5288del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.107_116del MANE Select ENSP00000358903.3:p.Leu36ProfsTer?
ENST00000638190.1:c.107_116del ENSP00000492539.1:p.Leu36ProfsTer?
ENST00000638272.1:c.107_116del ENSP00000491508.1:p.Leu36ProfsTer?
ENST00000638971.1:c.107_116del ENSP00000492313.1:p.Leu36ProfsTer?
ENST00000639393.1:c.107_116del ENSP00000492651.1:p.Leu36ProfsTer?
ENST00000369887.3:c.107_116del ENSP00000358903.3:p.Leu36ProfsTer?
ENST00000489268.1:n.160_169del
NM_000102.3:c.107_116del NP_000093.1:p.Leu36ProfsTer?
NM_000102.4:c.107_116del MANE Select NP_000093.1:p.Leu36ProfsTer?