Canonical Allele Identifier: CA377938665
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104592274T>A (hg19) chr10:g.102832517T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832517T>A , CM000672.2:g.102832517T>A GRCh38
NC_000010.10:g.104592274T>A , CM000672.1:g.104592274T>A GRCh37
NC_000010.9:g.104582264T>A NCBI36
NG_007955.1:g.10017A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.1133A>T (CYP17A1) MANE Select ENSP00000358903.3:p.Asp378Val
ENST00000638190.1:c.830A>T (CYP17A1) ENSP00000492539.1:p.Asp277Val
ENST00000638272.1:c.677A>T (CYP17A1) ENSP00000491508.1:p.Asp226Val
ENST00000638971.1:c.1046A>T (CYP17A1) ENSP00000492313.1:p.Asp349Val
ENST00000639393.1:c.1133A>T (CYP17A1) ENSP00000492651.1:p.Asp378Val
ENST00000640633.1:n.895A>T (CYP17A1)
ENST00000647664.1:c.*1548T>A (WBP1L) ENSP00000498131.1:n.*1548T>A
ENST00000369887.3:c.1133A>T (CYP17A1) ENSP00000358903.3:p.Asp378Val
NM_000102.3:c.1133A>T (CYP17A1) NP_000093.1:p.Asp378Val
NM_000102.4:c.1133A>T (CYP17A1) MANE Select NP_000093.1:p.Asp378Val
Search 100 bp 5'
Search 100 bp 3'