Canonical Allele Identifier: CA377938890

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104592383G>A (hg19) ; chr10:g.102832626G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832626G>A , CM000672.2:g.102832626G>A	GRCh38
NC_000010.10:g.104592383G>A , CM000672.1:g.104592383G>A	GRCh37
NC_000010.9:g.104582373G>A	NCBI36
NG_007955.1:g.9908C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1024C>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Pro342Ser
ENST00000638190.1:c.721C>T (CYP17A1)	ENSP00000492539.1:p.Pro241Ser
ENST00000638272.1:c.568C>T (CYP17A1)	ENSP00000491508.1:p.Pro190Ser
ENST00000638971.1:c.937C>T (CYP17A1)	ENSP00000492313.1:p.Pro313Ser
ENST00000639393.1:c.1024C>T (CYP17A1)	ENSP00000492651.1:p.Pro342Ser
ENST00000640633.1:n.786C>T (CYP17A1)
ENST00000647664.1:c.*1657G>A (WBP1L)	ENSP00000498131.1:n.*1657G>A
ENST00000369887.3:c.1024C>T (CYP17A1)	ENSP00000358903.3:p.Pro342Ser
NM_000102.3:c.1024C>T (CYP17A1)	NP_000093.1:p.Pro342Ser
NM_000102.4:c.1024C>T (CYP17A1) MANE Select	NP_000093.1:p.Pro342Ser