Canonical Allele Identifier: CA5669622
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs770800801

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837110C>G , CM000672.2:g.102837110C>G GRCh38
NC_000010.10:g.104596867C>G , CM000672.1:g.104596867C>G GRCh37
NC_000010.9:g.104586857C>G NCBI36
NG_007955.1:g.5424G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.252G>C MANE Select ENSP00000358903.3:p.Glu84Asp
ENST00000638190.1:c.252G>C ENSP00000492539.1:p.Glu84Asp
ENST00000638272.1:c.252G>C ENSP00000491508.1:p.Glu84Asp
ENST00000638971.1:c.252G>C ENSP00000492313.1:p.Glu84Asp
ENST00000639393.1:c.252G>C ENSP00000492651.1:p.Glu84Asp
ENST00000369887.3:c.252G>C ENSP00000358903.3:p.Glu84Asp
ENST00000489268.1:n.305G>C
NM_000102.3:c.252G>C NP_000093.1:p.Glu84Asp
NM_000102.4:c.252G>C MANE Select NP_000093.1:p.Glu84Asp