Canonical Allele Identifier: CA377940047
Gene: CYP17A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104594690A>C (hg19) chr10:g.102834933A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834933A>C , CM000672.2:g.102834933A>C GRCh38
NC_000010.10:g.104594690A>C , CM000672.1:g.104594690A>C GRCh37
NC_000010.9:g.104584680A>C NCBI36
NG_007955.1:g.7601T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.518T>G MANE Select ENSP00000358903.3:p.Val173Gly
ENST00000638190.1:c.518T>G ENSP00000492539.1:p.Val173Gly
ENST00000638272.1:c.298-1725T>G ENSP00000491508.1:n.298-1725T>G
ENST00000638971.1:c.518T>G ENSP00000492313.1:p.Val173Gly
ENST00000639393.1:c.518T>G ENSP00000492651.1:p.Val173Gly
ENST00000640633.1:n.280T>G
ENST00000369887.3:c.518T>G ENSP00000358903.3:p.Val173Gly
ENST00000489268.1:n.772T>G
NM_000102.3:c.518T>G NP_000093.1:p.Val173Gly
NM_000102.4:c.518T>G MANE Select NP_000093.1:p.Val173Gly
Search 100 bp 5'
Search 100 bp 3'