Canonical Allele Identifier: CA1932839725
Gene: CYP17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2873979
ClinVar RCV Id: RCV003712204
dbSNP Id: rs1590204152

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835399A>G , CM000672.2:g.102835399A>G GRCh38
NC_000010.10:g.104595156A>G , CM000672.1:g.104595156A>G GRCh37
NC_000010.9:g.104585146A>G NCBI36
NG_007955.1:g.7135T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.298-7T>C MANE Select ENSP00000358903.3:n.298-7T>C
ENST00000638190.1:c.298-7T>C ENSP00000492539.1:n.298-7T>C
ENST00000638272.1:c.297+1666T>C ENSP00000491508.1:n.297+1666T>C
ENST00000638971.1:c.298-7T>C ENSP00000492313.1:n.298-7T>C
ENST00000639393.1:c.298-7T>C ENSP00000492651.1:n.298-7T>C
ENST00000640633.1:n.60-7T>C
ENST00000369887.3:c.298-7T>C ENSP00000358903.3:n.298-7T>C
ENST00000489268.1:n.545T>C
NM_000102.3:c.298-7T>C NP_000093.1:n.298-7T>C
NM_000102.4:c.298-7T>C MANE Select NP_000093.1:n.298-7T>C