Canonical Allele Identifier: CA5669453
Community Standard Title: NM_000102.4(CYP17A1):c.887T>C (p.Ile296Thr)
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102833075A>G , CM000672.2:g.102833075A>G GRCh38
NC_000010.10:g.104592832A>G , CM000672.1:g.104592832A>G GRCh37
NC_000010.9:g.104582822A>G NCBI36
NG_007955.1:g.9459T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000102.4:c.887T>C (CYP17A1) MANE Select NP_000093.1:p.Ile296Thr
ENST00000369887.4:c.887T>C (CYP17A1) MANE Select ENSP00000358903.3:p.Ile296Thr
NM_000102.3:c.887T>C (CYP17A1) NP_000093.1:p.Ile296Thr
ENST00000369884.4:n.151+204A>G
ENST00000369887.3:c.887T>C (CYP17A1) ENSP00000358903.3:p.Ile296Thr
ENST00000638190.1:c.667-395T>C (CYP17A1) ENSP00000492539.1:n.667-395T>C
ENST00000638272.1:c.431T>C (CYP17A1) ENSP00000491508.1:p.Ile144Thr
ENST00000638971.1:c.800T>C (CYP17A1) ENSP00000492313.1:p.Ile267Thr
ENST00000639393.1:c.887T>C (CYP17A1) ENSP00000492651.1:p.Ile296Thr
ENST00000640633.1:n.649T>C (CYP17A1)
ENST00000647664.1:c.*2106A>G (WBP1L) ENSP00000498131.1:n.*2106A>G
XR_428804.1:n.205+204A>G (CYP17A1-AS1)