Canonical Allele Identifier: CA377938219

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104590661C>G (hg19) ; chr10:g.102830904C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830904C>G , CM000672.2:g.102830904C>G	GRCh38
NC_000010.10:g.104590661C>G , CM000672.1:g.104590661C>G	GRCh37
NC_000010.9:g.104580651C>G	NCBI36
NG_007955.1:g.11630G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1325G>C (CYP17A1) MANE Select	ENSP00000358903.3:p.Cys442Ser
ENST00000638190.1:c.1022G>C (CYP17A1)	ENSP00000492539.1:p.Cys341Ser
ENST00000638272.1:c.869G>C (CYP17A1)	ENSP00000491508.1:p.Cys290Ser
ENST00000638971.1:c.1238G>C (CYP17A1)	ENSP00000492313.1:p.Cys413Ser
ENST00000639393.1:c.1328G>C (CYP17A1)	ENSP00000492651.1:p.Cys443Ser
ENST00000640633.1:n.1087G>C (CYP17A1)
ENST00000647664.1:c.*586C>G (WBP1L)	ENSP00000498131.1:n.*586C>G
ENST00000369887.3:c.1325G>C (CYP17A1)	ENSP00000358903.3:p.Cys442Ser
NM_000102.3:c.1325G>C (CYP17A1)	NP_000093.1:p.Cys442Ser
NM_000102.4:c.1325G>C (CYP17A1) MANE Select	NP_000093.1:p.Cys442Ser