Canonical Allele Identifier: CA377938657
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832514G>A , CM000672.2:g.102832514G>A GRCh38
NC_000010.10:g.104592271G>A , CM000672.1:g.104592271G>A GRCh37
NC_000010.9:g.104582261G>A NCBI36
NG_007955.1:g.10020C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.1136C>T (CYP17A1) MANE Select ENSP00000358903.3:p.Ser379Phe
ENST00000638190.1:c.833C>T (CYP17A1) ENSP00000492539.1:p.Ser278Phe
ENST00000638272.1:c.680C>T (CYP17A1) ENSP00000491508.1:p.Ser227Phe
ENST00000638971.1:c.1049C>T (CYP17A1) ENSP00000492313.1:p.Ser350Phe
ENST00000639393.1:c.1136C>T (CYP17A1) ENSP00000492651.1:p.Ser379Phe
ENST00000640633.1:n.898C>T (CYP17A1)
ENST00000647664.1:c.*1545G>A (WBP1L) ENSP00000498131.1:n.*1545G>A
ENST00000369887.3:c.1136C>T (CYP17A1) ENSP00000358903.3:p.Ser379Phe
NM_000102.3:c.1136C>T (CYP17A1) NP_000093.1:p.Ser379Phe
NM_000102.4:c.1136C>T (CYP17A1) MANE Select NP_000093.1:p.Ser379Phe