Canonical Allele Identifier: CA377938224
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

dbSNP Id: rs1844078988

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102830907G>A , CM000672.2:g.102830907G>A GRCh38
NC_000010.10:g.104590664G>A , CM000672.1:g.104590664G>A GRCh37
NC_000010.9:g.104580654G>A NCBI36
NG_007955.1:g.11627C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.1322C>T (CYP17A1) MANE Select ENSP00000358903.3:p.Ser441Phe
ENST00000638190.1:c.1019C>T (CYP17A1) ENSP00000492539.1:p.Ser340Phe
ENST00000638272.1:c.866C>T (CYP17A1) ENSP00000491508.1:p.Ser289Phe
ENST00000638971.1:c.1235C>T (CYP17A1) ENSP00000492313.1:p.Ser412Phe
ENST00000639393.1:c.1325C>T (CYP17A1) ENSP00000492651.1:p.Ser442Phe
ENST00000640633.1:n.1084C>T (CYP17A1)
ENST00000647664.1:c.*589G>A (WBP1L) ENSP00000498131.1:n.*589G>A
ENST00000369887.3:c.1322C>T (CYP17A1) ENSP00000358903.3:p.Ser441Phe
NM_000102.3:c.1322C>T (CYP17A1) NP_000093.1:p.Ser441Phe
NM_000102.4:c.1322C>T (CYP17A1) MANE Select NP_000093.1:p.Ser441Phe