Canonical Allele Identifier: CA5669542
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs757454955

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834958T>C , CM000672.2:g.102834958T>C GRCh38
NC_000010.10:g.104594715T>C , CM000672.1:g.104594715T>C GRCh37
NC_000010.9:g.104584705T>C NCBI36
NG_007955.1:g.7576A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.493A>G MANE Select ENSP00000358903.3:p.Ile165Val
ENST00000638190.1:c.493A>G ENSP00000492539.1:p.Ile165Val
ENST00000638272.1:c.298-1750A>G ENSP00000491508.1:n.298-1750A>G
ENST00000638971.1:c.493A>G ENSP00000492313.1:p.Ile165Val
ENST00000639393.1:c.493A>G ENSP00000492651.1:p.Ile165Val
ENST00000640633.1:n.255A>G
ENST00000369887.3:c.493A>G ENSP00000358903.3:p.Ile165Val
ENST00000489268.1:n.747A>G
NM_000102.3:c.493A>G NP_000093.1:p.Ile165Val
NM_000102.4:c.493A>G MANE Select NP_000093.1:p.Ile165Val