Canonical Allele Identifier: CA1932839684

Gene: CYP17A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102835368_102835369delinsTG , CM000672.2:g.102835368_102835369delinsTG	GRCh38
NC_000010.10:g.104595125_104595126delinsTG , CM000672.1:g.104595125_104595126delinsTG	GRCh37
NC_000010.9:g.104585115_104585116delinsTG	NCBI36
NG_007955.1:g.7165_7166delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.321_322delinsCA MANE Select	ENSP00000358903.3:p.Asn107=
ENST00000638190.1:c.321_322delinsCA	ENSP00000492539.1:p.Asn107=
ENST00000638272.1:c.297+1696_297+1697delinsCA	ENSP00000491508.1:n.297+1696_297+1697delinsCA
ENST00000638971.1:c.321_322delinsCA	ENSP00000492313.1:p.Asn107=
ENST00000639393.1:c.321_322delinsCA	ENSP00000492651.1:p.Asn107=
ENST00000640633.1:n.83_84delinsCA
ENST00000369887.3:c.321_322delinsCA	ENSP00000358903.3:p.Asn107=
ENST00000489268.1:n.575_576delinsCA
NM_000102.3:c.321_322delinsCA	NP_000093.1:p.Asn107=
NM_000102.4:c.321_322delinsCA MANE Select	NP_000093.1:p.Asn107=