Canonical Allele Identifier: CA2739275962
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2787239
ClinVar RCV Id: RCV003660643
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834765C>T , CM000672.2:g.102834765C>T GRCh38
NC_000010.10:g.104594522C>T , CM000672.1:g.104594522C>T GRCh37
NC_000010.9:g.104584512C>T NCBI36
NG_007955.1:g.7769G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.666+20G>A MANE Select ENSP00000358903.3:n.666+20G>A
ENST00000638190.1:c.666+20G>A ENSP00000492539.1:n.666+20G>A
ENST00000638272.1:c.298-1557G>A ENSP00000491508.1:n.298-1557G>A
ENST00000638971.1:c.666+20G>A ENSP00000492313.1:n.666+20G>A
ENST00000639393.1:c.666+20G>A ENSP00000492651.1:n.666+20G>A
ENST00000640633.1:n.428+20G>A
ENST00000369887.3:c.666+20G>A ENSP00000358903.3:n.666+20G>A
ENST00000489268.1:n.940G>A
NM_000102.3:c.666+20G>A NP_000093.1:n.666+20G>A
NM_000102.4:c.666+20G>A MANE Select NP_000093.1:n.666+20G>A
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