Canonical Allele Identifier: CA1932870888
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832671T= , CM000672.2:g.102832671T= GRCh38
NC_000010.10:g.104592428T= , CM000672.1:g.104592428T= GRCh37
NC_000010.9:g.104582418T= NCBI36
NG_007955.1:g.9863A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.979A= (CYP17A1) MANE Select ENSP00000358903.3:p.Lys327=
ENST00000638190.1:c.676A= (CYP17A1) ENSP00000492539.1:p.Lys226=
ENST00000638272.1:c.523A= (CYP17A1) ENSP00000491508.1:p.Lys175=
ENST00000638971.1:c.892A= (CYP17A1) ENSP00000492313.1:p.Lys298=
ENST00000639393.1:c.979A= (CYP17A1) ENSP00000492651.1:p.Lys327=
ENST00000640633.1:n.741A= (CYP17A1)
ENST00000647664.1:c.*1702T= (WBP1L) ENSP00000498131.1:n.*1702T=
ENST00000369887.3:c.979A= (CYP17A1) ENSP00000358903.3:p.Lys327=
NM_000102.3:c.979A= (CYP17A1) NP_000093.1:p.Lys327=
XR_428804.1:n.5T= (CYP17A1-AS1)
NM_000102.4:c.979A= (CYP17A1) MANE Select NP_000093.1:p.Lys327=