Canonical Allele Identifier: CA1932873565
Gene: CYP17A1 HGNC NCBI
CYP17A1-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102833925G= , CM000672.2:g.102833925G= GRCh38
NC_000010.10:g.104593682G= , CM000672.1:g.104593682G= GRCh37
NC_000010.9:g.104583672G= NCBI36
NG_007955.1:g.8609C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369884.4:n.152-252G=
ENST00000369887.4:c.753+111C= (CYP17A1) MANE Select ENSP00000358903.3:n.753+111C=
ENST00000638190.1:c.666+860C= (CYP17A1) ENSP00000492539.1:n.666+860C=
ENST00000638272.1:c.298-717C= (CYP17A1) ENSP00000491508.1:n.298-717C=
ENST00000638971.1:c.667-717C= (CYP17A1) ENSP00000492313.1:n.667-717C=
ENST00000639393.1:c.753+111C= (CYP17A1) ENSP00000492651.1:n.753+111C=
ENST00000640633.1:n.515+111C= (CYP17A1)
ENST00000369887.3:c.753+111C= (CYP17A1) ENSP00000358903.3:n.753+111C=
ENST00000489268.1:n.1780C= (CYP17A1)
NM_000102.3:c.753+111C= (CYP17A1) NP_000093.1:n.753+111C=
XR_428804.1:n.206-252G= (CYP17A1-AS1)
NM_000102.4:c.753+111C= (CYP17A1) MANE Select NP_000093.1:n.753+111C=
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