Canonical Allele Identifier: CA1932868340
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102831454G= , CM000672.2:g.102831454G= GRCh38
NC_000010.10:g.104591211G= , CM000672.1:g.104591211G= GRCh37
NC_000010.9:g.104581201G= NCBI36
NG_007955.1:g.11080C=

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.1243+54C= (CYP17A1) MANE Select ENSP00000358903.3:n.1243+54C=
ENST00000638190.1:c.940+54C= (CYP17A1) ENSP00000492539.1:n.940+54C=
ENST00000638272.1:c.787+54C= (CYP17A1) ENSP00000491508.1:n.787+54C=
ENST00000638971.1:c.1156+54C= (CYP17A1) ENSP00000492313.1:n.1156+54C=
ENST00000639393.1:c.1246+54C= (CYP17A1) ENSP00000492651.1:n.1246+54C=
ENST00000640633.1:n.1005+54C= (CYP17A1)
ENST00000647664.1:c.*629-144G= (WBP1L) ENSP00000498131.1:n.*629-144G=
ENST00000369887.3:c.1243+54C= (CYP17A1) ENSP00000358903.3:n.1243+54C=
ENST00000469683.1:n.196+54C= (CYP17A1)
NM_000102.3:c.1243+54C= (CYP17A1) NP_000093.1:n.1243+54C=
NM_000102.4:c.1243+54C= (CYP17A1) MANE Select NP_000093.1:n.1243+54C=