Canonical Allele Identifier: CA377940657
Gene: CYP17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837112C>G , CM000672.2:g.102837112C>G GRCh38
NC_000010.10:g.104596869C>G , CM000672.1:g.104596869C>G GRCh37
NC_000010.9:g.104586859C>G NCBI36
NG_007955.1:g.5422G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.250G>C MANE Select ENSP00000358903.3:p.Glu84Gln
ENST00000638190.1:c.250G>C ENSP00000492539.1:p.Glu84Gln
ENST00000638272.1:c.250G>C ENSP00000491508.1:p.Glu84Gln
ENST00000638971.1:c.250G>C ENSP00000492313.1:p.Glu84Gln
ENST00000639393.1:c.250G>C ENSP00000492651.1:p.Glu84Gln
ENST00000369887.3:c.250G>C ENSP00000358903.3:p.Glu84Gln
ENST00000489268.1:n.303G>C
NM_000102.3:c.250G>C NP_000093.1:p.Glu84Gln
NM_000102.4:c.250G>C MANE Select NP_000093.1:p.Glu84Gln