Canonical Allele Identifier: CA377939012
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832679A>C , CM000672.2:g.102832679A>C GRCh38
NC_000010.10:g.104592436A>C , CM000672.1:g.104592436A>C GRCh37
NC_000010.9:g.104582426A>C NCBI36
NG_007955.1:g.9855T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.971T>G (CYP17A1) MANE Select ENSP00000358903.3:p.Val324Gly
ENST00000638190.1:c.668T>G (CYP17A1) ENSP00000492539.1:p.Val223Gly
ENST00000638272.1:c.515T>G (CYP17A1) ENSP00000491508.1:p.Val172Gly
ENST00000638971.1:c.884T>G (CYP17A1) ENSP00000492313.1:p.Val295Gly
ENST00000639393.1:c.971T>G (CYP17A1) ENSP00000492651.1:p.Val324Gly
ENST00000640633.1:n.733T>G (CYP17A1)
ENST00000647664.1:c.*1710A>C (WBP1L) ENSP00000498131.1:n.*1710A>C
ENST00000369887.3:c.971T>G (CYP17A1) ENSP00000358903.3:p.Val324Gly
NM_000102.3:c.971T>G (CYP17A1) NP_000093.1:p.Val324Gly
XR_428804.1:n.13A>C (CYP17A1-AS1)
NM_000102.4:c.971T>G (CYP17A1) MANE Select NP_000093.1:p.Val324Gly