Canonical Allele Identifier: CA377938687
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832527C>G , CM000672.2:g.102832527C>G GRCh38
NC_000010.10:g.104592284C>G , CM000672.1:g.104592284C>G GRCh37
NC_000010.9:g.104582274C>G NCBI36
NG_007955.1:g.10007G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.1123G>C (CYP17A1) MANE Select ENSP00000358903.3:p.Ala375Pro
ENST00000638190.1:c.820G>C (CYP17A1) ENSP00000492539.1:p.Ala274Pro
ENST00000638272.1:c.667G>C (CYP17A1) ENSP00000491508.1:p.Ala223Pro
ENST00000638971.1:c.1036G>C (CYP17A1) ENSP00000492313.1:p.Ala346Pro
ENST00000639393.1:c.1123G>C (CYP17A1) ENSP00000492651.1:p.Ala375Pro
ENST00000640633.1:n.885G>C (CYP17A1)
ENST00000647664.1:c.*1558C>G (WBP1L) ENSP00000498131.1:n.*1558C>G
ENST00000369887.3:c.1123G>C (CYP17A1) ENSP00000358903.3:p.Ala375Pro
NM_000102.3:c.1123G>C (CYP17A1) NP_000093.1:p.Ala375Pro
NM_000102.4:c.1123G>C (CYP17A1) MANE Select NP_000093.1:p.Ala375Pro