Canonical Allele Identifier: CA1932873706
Gene: CYP17A1 HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102833966G= , CM000672.2:g.102833966G= GRCh38
NC_000010.10:g.104593723G= , CM000672.1:g.104593723G= GRCh37
NC_000010.9:g.104583713G= NCBI36
NG_007955.1:g.8568C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369884.4:n.152-211G=
ENST00000369887.4:c.753+70C= (CYP17A1) MANE Select ENSP00000358903.3:n.753+70C=
ENST00000638190.1:c.666+819C= (CYP17A1) ENSP00000492539.1:n.666+819C=
ENST00000638272.1:c.298-758C= (CYP17A1) ENSP00000491508.1:n.298-758C=
ENST00000638971.1:c.667-758C= (CYP17A1) ENSP00000492313.1:n.667-758C=
ENST00000639393.1:c.753+70C= (CYP17A1) ENSP00000492651.1:n.753+70C=
ENST00000640633.1:n.515+70C= (CYP17A1)
ENST00000369887.3:c.753+70C= (CYP17A1) ENSP00000358903.3:n.753+70C=
ENST00000489268.1:n.1739C= (CYP17A1)
NM_000102.3:c.753+70C= (CYP17A1) NP_000093.1:n.753+70C=
XR_428804.1:n.206-211G= (CYP17A1-AS1)
NM_000102.4:c.753+70C= (CYP17A1) MANE Select NP_000093.1:n.753+70C=