Canonical Allele Identifier: CA1932874168
Gene: CYP17A1 HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834151A= , CM000672.2:g.102834151A= GRCh38
NC_000010.10:g.104593908A= , CM000672.1:g.104593908A= GRCh37
NC_000010.9:g.104583898A= NCBI36
NG_007955.1:g.8383T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369884.4:n.152-26A=
ENST00000369887.4:c.667-29T= (CYP17A1) MANE Select ENSP00000358903.3:n.667-29T=
ENST00000638190.1:c.666+634T= (CYP17A1) ENSP00000492539.1:n.666+634T=
ENST00000638272.1:c.298-943T= (CYP17A1) ENSP00000491508.1:n.298-943T=
ENST00000638971.1:c.666+634T= (CYP17A1) ENSP00000492313.1:n.666+634T=
ENST00000639393.1:c.667-29T= (CYP17A1) ENSP00000492651.1:n.667-29T=
ENST00000640633.1:n.429-29T= (CYP17A1)
ENST00000369887.3:c.667-29T= (CYP17A1) ENSP00000358903.3:n.667-29T=
ENST00000489268.1:n.1554T= (CYP17A1)
NM_000102.3:c.667-29T= (CYP17A1) NP_000093.1:n.667-29T=
XR_428804.1:n.206-26A= (CYP17A1-AS1)
NM_000102.4:c.667-29T= (CYP17A1) MANE Select NP_000093.1:n.667-29T=