Canonical Allele Identifier: CA471297433
Gene: CYP17A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104594583del (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834827del , CM000672.2:g.102834827del GRCh38
NC_000010.10:g.104594584del , CM000672.1:g.104594584del GRCh37
NC_000010.9:g.104584574del NCBI36
NG_007955.1:g.7708del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.625del MANE Select ENSP00000358903.3:p.Leu209Ter
ENST00000638190.1:c.625del ENSP00000492539.1:p.Leu209Ter
ENST00000638272.1:c.298-1618del ENSP00000491508.1:n.298-1618del
ENST00000638971.1:c.625del ENSP00000492313.1:p.Leu209Ter
ENST00000639393.1:c.625del ENSP00000492651.1:p.Leu209Ter
ENST00000640633.1:n.387del
ENST00000369887.3:c.625del ENSP00000358903.3:p.Leu209Ter
ENST00000489268.1:n.879del
NM_000102.3:c.625del NP_000093.1:p.Leu209Ter
NM_000102.4:c.625del MANE Select NP_000093.1:p.Leu209Ter
Search 100 bp 5'
Search 100 bp 3'