Canonical Allele Identifier: CA2610725253
Gene: CYP17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102836817_102836822del , CM000672.2:g.102836817_102836822del GRCh38
NC_000010.10:g.104596574_104596579del , CM000672.1:g.104596574_104596579del GRCh37
NC_000010.9:g.104586564_104586569del NCBI36
NG_007955.1:g.5712_5717del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.297+243_297+248del MANE Select ENSP00000358903.3:n.297+243_297+248del
ENST00000638190.1:c.297+243_297+248del ENSP00000492539.1:n.297+243_297+248del
ENST00000638272.1:c.297+243_297+248del ENSP00000491508.1:n.297+243_297+248del
ENST00000638971.1:c.297+243_297+248del ENSP00000492313.1:n.297+243_297+248del
ENST00000639393.1:c.297+243_297+248del ENSP00000492651.1:n.297+243_297+248del
ENST00000369887.3:c.297+243_297+248del ENSP00000358903.3:n.297+243_297+248del
ENST00000489268.1:n.350+243_350+248del
NM_000102.3:c.297+243_297+248del NP_000093.1:n.297+243_297+248del
NM_000102.4:c.297+243_297+248del MANE Select NP_000093.1:n.297+243_297+248del