Canonical Allele Identifier: CA377938689
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832528C>A , CM000672.2:g.102832528C>A GRCh38
NC_000010.10:g.104592285C>A , CM000672.1:g.104592285C>A GRCh37
NC_000010.9:g.104582275C>A NCBI36
NG_007955.1:g.10006G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.1122G>T (CYP17A1) MANE Select ENSP00000358903.3:p.Lys374Asn
ENST00000638190.1:c.819G>T (CYP17A1) ENSP00000492539.1:p.Lys273Asn
ENST00000638272.1:c.666G>T (CYP17A1) ENSP00000491508.1:p.Lys222Asn
ENST00000638971.1:c.1035G>T (CYP17A1) ENSP00000492313.1:p.Lys345Asn
ENST00000639393.1:c.1122G>T (CYP17A1) ENSP00000492651.1:p.Lys374Asn
ENST00000640633.1:n.884G>T (CYP17A1)
ENST00000647664.1:c.*1559C>A (WBP1L) ENSP00000498131.1:n.*1559C>A
ENST00000369887.3:c.1122G>T (CYP17A1) ENSP00000358903.3:p.Lys374Asn
NM_000102.3:c.1122G>T (CYP17A1) NP_000093.1:p.Lys374Asn
NM_000102.4:c.1122G>T (CYP17A1) MANE Select NP_000093.1:p.Lys374Asn