Canonical Allele Identifier: CA1932870953
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1844106810

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832704del , CM000672.2:g.102832704del GRCh38
NC_000010.10:g.104592461del , CM000672.1:g.104592461del GRCh37
NC_000010.9:g.104582451del NCBI36
NG_007955.1:g.9831del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.970-23del (CYP17A1) MANE Select ENSP00000358903.3:n.970-23del
ENST00000638190.1:c.667-23del (CYP17A1) ENSP00000492539.1:n.667-23del
ENST00000638272.1:c.514-23del (CYP17A1) ENSP00000491508.1:n.514-23del
ENST00000638971.1:c.883-23del (CYP17A1) ENSP00000492313.1:n.883-23del
ENST00000639393.1:c.970-23del (CYP17A1) ENSP00000492651.1:n.970-23del
ENST00000640633.1:n.732-23del (CYP17A1)
ENST00000647664.1:c.*1735del (WBP1L) ENSP00000498131.1:n.*1735del
ENST00000369887.3:c.970-23del (CYP17A1) ENSP00000358903.3:n.970-23del
NM_000102.3:c.970-23del (CYP17A1) NP_000093.1:n.970-23del
XR_428804.1:n.38del (CYP17A1-AS1)
NM_000102.4:c.970-23del (CYP17A1) MANE Select NP_000093.1:n.970-23del