Canonical Allele Identifier: CA377938992
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104592428T>C (hg19) chr10:g.102832671T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832671T>C , CM000672.2:g.102832671T>C GRCh38
NC_000010.10:g.104592428T>C , CM000672.1:g.104592428T>C GRCh37
NC_000010.9:g.104582418T>C NCBI36
NG_007955.1:g.9863A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.979A>G (CYP17A1) MANE Select ENSP00000358903.3:p.Lys327Glu
ENST00000638190.1:c.676A>G (CYP17A1) ENSP00000492539.1:p.Lys226Glu
ENST00000638272.1:c.523A>G (CYP17A1) ENSP00000491508.1:p.Lys175Glu
ENST00000638971.1:c.892A>G (CYP17A1) ENSP00000492313.1:p.Lys298Glu
ENST00000639393.1:c.979A>G (CYP17A1) ENSP00000492651.1:p.Lys327Glu
ENST00000640633.1:n.741A>G (CYP17A1)
ENST00000647664.1:c.*1702T>C (WBP1L) ENSP00000498131.1:n.*1702T>C
ENST00000369887.3:c.979A>G (CYP17A1) ENSP00000358903.3:p.Lys327Glu
NM_000102.3:c.979A>G (CYP17A1) NP_000093.1:p.Lys327Glu
XR_428804.1:n.5T>C (CYP17A1-AS1)
NM_000102.4:c.979A>G (CYP17A1) MANE Select NP_000093.1:p.Lys327Glu
Search 100 bp 5'
Search 100 bp 3'