Canonical Allele Identifier: CA1932841275
Gene: CYP17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837245_102837255delinsGCTGCCCACCA , CM000672.2:g.102837245_102837255delinsGCTGCCCACCA GRCh38
NC_000010.10:g.104597002_104597012delinsGCTGCCCACCA , CM000672.1:g.104597002_104597012delinsGCTGCCCACCA GRCh37
NC_000010.9:g.104586992_104587002delinsGCTGCCCACCA NCBI36
NG_007955.1:g.5279_5289delinsTGGTGGGCAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.107_117delinsTGGTGGGCAGC MANE Select ENSP00000358903.3:p.Leu36=
ENST00000638190.1:c.107_117delinsTGGTGGGCAGC ENSP00000492539.1:p.Leu36=
ENST00000638272.1:c.107_117delinsTGGTGGGCAGC ENSP00000491508.1:p.Leu36=
ENST00000638971.1:c.107_117delinsTGGTGGGCAGC ENSP00000492313.1:p.Leu36=
ENST00000639393.1:c.107_117delinsTGGTGGGCAGC ENSP00000492651.1:p.Leu36=
ENST00000369887.3:c.107_117delinsTGGTGGGCAGC ENSP00000358903.3:p.Leu36=
ENST00000489268.1:n.160_170delinsTGGTGGGCAGC
NM_000102.3:c.107_117delinsTGGTGGGCAGC NP_000093.1:p.Leu36=
NM_000102.4:c.107_117delinsTGGTGGGCAGC MANE Select NP_000093.1:p.Leu36=