Canonical Allele Identifier: CA377938658
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.1136C>G (CYP17A1) MANE Select ENSP00000358903.3:p.Ser379Cys
ENST00000638190.1:c.833C>G (CYP17A1) ENSP00000492539.1:p.Ser278Cys
ENST00000638272.1:c.680C>G (CYP17A1) ENSP00000491508.1:p.Ser227Cys
ENST00000638971.1:c.1049C>G (CYP17A1) ENSP00000492313.1:p.Ser350Cys
ENST00000639393.1:c.1136C>G (CYP17A1) ENSP00000492651.1:p.Ser379Cys
ENST00000640633.1:n.898C>G (CYP17A1)
ENST00000647664.1:c.*1545G>C (WBP1L) ENSP00000498131.1:n.*1545G>C
ENST00000369887.3:c.1136C>G (CYP17A1) ENSP00000358903.3:p.Ser379Cys
NM_000102.3:c.1136C>G (CYP17A1) NP_000093.1:p.Ser379Cys
NM_000102.4:c.1136C>G (CYP17A1) MANE Select NP_000093.1:p.Ser379Cys