Canonical Allele Identifier: CA377940881
Gene: CYP17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837214G>C , CM000672.2:g.102837214G>C GRCh38
NC_000010.10:g.104596971G>C , CM000672.1:g.104596971G>C GRCh37
NC_000010.9:g.104586961G>C NCBI36
NG_007955.1:g.5320C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.148C>G MANE Select ENSP00000358903.3:p.His50Asp
ENST00000638190.1:c.148C>G ENSP00000492539.1:p.His50Asp
ENST00000638272.1:c.148C>G ENSP00000491508.1:p.His50Asp
ENST00000638971.1:c.148C>G ENSP00000492313.1:p.His50Asp
ENST00000639393.1:c.148C>G ENSP00000492651.1:p.His50Asp
ENST00000369887.3:c.148C>G ENSP00000358903.3:p.His50Asp
ENST00000489268.1:n.201C>G
NM_000102.3:c.148C>G NP_000093.1:p.His50Asp
NM_000102.4:c.148C>G MANE Select NP_000093.1:p.His50Asp