Canonical Allele Identifier: CA1932875458
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834671_102834672delinsTA , CM000672.2:g.102834671_102834672delinsTA GRCh38
NC_000010.10:g.104594428_104594429delinsTA , CM000672.1:g.104594428_104594429delinsTA GRCh37
NC_000010.9:g.104584418_104584419delinsTA NCBI36
NG_007955.1:g.7862_7863delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.666+113_666+114delinsTA MANE Select ENSP00000358903.3:n.666+113_666+114delins...
ENST00000638190.1:c.666+113_666+114delinsTA ENSP00000492539.1:n.666+113_666+114delins...
ENST00000638272.1:c.298-1464_298-1463delinsTA ENSP00000491508.1:n.298-1464_298-1463deli...
ENST00000638971.1:c.666+113_666+114delinsTA ENSP00000492313.1:n.666+113_666+114delins...
ENST00000639393.1:c.666+113_666+114delinsTA ENSP00000492651.1:n.666+113_666+114delins...
ENST00000640633.1:n.428+113_428+114delinsTA
ENST00000369887.3:c.666+113_666+114delinsTA ENSP00000358903.3:n.666+113_666+114delins...
ENST00000489268.1:n.1033_1034delinsTA
NM_000102.3:c.666+113_666+114delinsTA NP_000093.1:n.666+113_666+114delinsTA
NM_000102.4:c.666+113_666+114delinsTA MANE Select NP_000093.1:n.666+113_666+114delinsTA