Canonical Allele Identifier: CA645568104
Gene: CYP17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837245del , CM000672.2:g.102837245del GRCh38
NC_000010.10:g.104597002del , CM000672.1:g.104597002del GRCh37
NC_000010.9:g.104586992del NCBI36
NG_007955.1:g.5290del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.118del MANE Select ENSP00000358903.3:p.Leu40CysfsTer?
ENST00000638190.1:c.118del ENSP00000492539.1:p.Leu40CysfsTer?
ENST00000638272.1:c.118del ENSP00000491508.1:p.Leu40CysfsTer?
ENST00000638971.1:c.118del ENSP00000492313.1:p.Leu40CysfsTer?
ENST00000639393.1:c.118del ENSP00000492651.1:p.Leu40CysfsTer?
ENST00000369887.3:c.118del ENSP00000358903.3:p.Leu40CysfsTer?
ENST00000489268.1:n.171del
NM_000102.3:c.118del NP_000093.1:p.Leu40CysfsTer?
NM_000102.4:c.118del MANE Select NP_000093.1:p.Leu40CysfsTer?