Canonical Allele Identifier: CA659060436
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs1207954426

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102836653_102836655dup , CM000672.2:g.102836653_102836655dup GRCh38
NC_000010.10:g.104596410_104596412dup , CM000672.1:g.104596410_104596412dup GRCh37
NC_000010.9:g.104586400_104586402dup NCBI36
NG_007955.1:g.5879_5881dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.297+410_297+412dup MANE Select ENSP00000358903.3:n.297+410_297+412dup
ENST00000638190.1:c.297+410_297+412dup ENSP00000492539.1:n.297+410_297+412dup
ENST00000638272.1:c.297+410_297+412dup ENSP00000491508.1:n.297+410_297+412dup
ENST00000638971.1:c.297+410_297+412dup ENSP00000492313.1:n.297+410_297+412dup
ENST00000639393.1:c.297+410_297+412dup ENSP00000492651.1:n.297+410_297+412dup
ENST00000640633.1:n.59+59_59+61dup
ENST00000369887.3:c.297+410_297+412dup ENSP00000358903.3:n.297+410_297+412dup
ENST00000489268.1:n.350+410_350+412dup
NM_000102.3:c.297+410_297+412dup NP_000093.1:n.297+410_297+412dup
NM_000102.4:c.297+410_297+412dup MANE Select NP_000093.1:n.297+410_297+412dup