Canonical Allele Identifier: CA1932873776
Gene: CYP17A1 HGNC NCBI
CYP17A1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834004_102834006delinsTAA , CM000672.2:g.102834004_102834006delinsTAA GRCh38
NC_000010.10:g.104593761_104593763delinsTAA , CM000672.1:g.104593761_104593763delinsTAA GRCh37
NC_000010.9:g.104583751_104583753delinsTAA NCBI36
NG_007955.1:g.8528_8530delinsTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000369884.4:n.152-173_152-171delinsTAA
ENST00000369887.4:c.753+30_753+32delinsTTA (CYP17A1) MANE Select ENSP00000358903.3:n.753+30_753+32delinsTT...
ENST00000638190.1:c.666+779_666+781delinsTTA (CYP17A1) ENSP00000492539.1:n.666+779_666+781delins...
ENST00000638272.1:c.298-798_298-796delinsTTA (CYP17A1) ENSP00000491508.1:n.298-798_298-796delins...
ENST00000638971.1:c.666+779_666+781delinsTTA (CYP17A1) ENSP00000492313.1:n.666+779_666+781delins...
ENST00000639393.1:c.753+30_753+32delinsTTA (CYP17A1) ENSP00000492651.1:n.753+30_753+32delinsTT...
ENST00000640633.1:n.515+30_515+32delinsTTA (CYP17A1)
ENST00000369887.3:c.753+30_753+32delinsTTA (CYP17A1) ENSP00000358903.3:n.753+30_753+32delinsTT...
ENST00000489268.1:n.1699_1701delinsTTA (CYP17A1)
NM_000102.3:c.753+30_753+32delinsTTA (CYP17A1) NP_000093.1:n.753+30_753+32delinsTTA
XR_428804.1:n.206-173_206-171delinsTAA (CYP17A1-AS1)
NM_000102.4:c.753+30_753+32delinsTTA (CYP17A1) MANE Select NP_000093.1:n.753+30_753+32delinsTTA