Canonical Allele Identifier: CA377938278
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104590690A>T (hg19) chr10:g.102830933A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102830933A>T , CM000672.2:g.102830933A>T GRCh38
NC_000010.10:g.104590690A>T , CM000672.1:g.104590690A>T GRCh37
NC_000010.9:g.104580680A>T NCBI36
NG_007955.1:g.11601T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.1296T>A (CYP17A1) MANE Select ENSP00000358903.3:p.Tyr432Ter
ENST00000638190.1:c.993T>A (CYP17A1) ENSP00000492539.1:p.Tyr331Ter
ENST00000638272.1:c.840T>A (CYP17A1) ENSP00000491508.1:p.Tyr280Ter
ENST00000638971.1:c.1209T>A (CYP17A1) ENSP00000492313.1:p.Tyr403Ter
ENST00000639393.1:c.1299T>A (CYP17A1) ENSP00000492651.1:p.Tyr433Ter
ENST00000640633.1:n.1058T>A (CYP17A1)
ENST00000647664.1:c.*615A>T (WBP1L) ENSP00000498131.1:n.*615A>T
ENST00000369887.3:c.1296T>A (CYP17A1) ENSP00000358903.3:p.Tyr432Ter
NM_000102.3:c.1296T>A (CYP17A1) NP_000093.1:p.Tyr432Ter
NM_000102.4:c.1296T>A (CYP17A1) MANE Select NP_000093.1:p.Tyr432Ter
Search 100 bp 5'
Search 100 bp 3'