Canonical Allele Identifier: CA115180
Gene: CYP17A1 HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1782
dbSNP Id: rs104894136

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834074G>A , CM000672.2:g.102834074G>A GRCh38
NC_000010.10:g.104593831G>A , CM000672.1:g.104593831G>A GRCh37
NC_000010.9:g.104583821G>A NCBI36
NG_007955.1:g.8460C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369884.4:n.152-103G>A
ENST00000369887.4:c.715C>T (CYP17A1) MANE Select ENSP00000358903.3:p.Arg239Ter
ENST00000638190.1:c.666+711C>T ENSP00000492539.1:p.=
ENST00000638272.1:c.298-866C>T ENSP00000491508.1:p.=
ENST00000638971.1:c.666+711C>T ENSP00000492313.1:p.=
ENST00000639393.1:c.715C>T ENSP00000492651.1:p.Arg239Ter
ENST00000640633.1:n.477C>T
ENST00000369887.3:c.715C>T ENSP00000358903.3:p.Arg239Ter
ENST00000489268.1:n.1631C>T
NM_000102.3:c.715C>T (CYP17A1) NP_000093.1:p.Arg239Ter
XR_428804.1:n.206-103G>A (CYP17A1-AS1)
NM_000102.4:c.715C>T (CYP17A1) MANE Select NP_000093.1:p.Arg239Ter