Canonical Allele Identifier: CA1932841508
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837450T= , CM000672.2:g.102837450T= GRCh38
NC_000010.10:g.104597207T= , CM000672.1:g.104597207T= GRCh37
NC_000010.9:g.104587197T= NCBI36
NG_007955.1:g.5084A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000638190.1:c.-89A= ENSP00000492539.1:n.-89A=
ENST00000638971.1:c.-89A= ENSP00000492313.1:n.-89A=
ENST00000369887.3:c.-89A= ENSP00000358903.3:n.-89A=
NM_000102.3:c.-89A= NP_000093.1:n.-89A=