Canonical Allele Identifier: CA2574686267
Gene: CYP17A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837045_102837046del , CM000672.2:g.102837045_102837046del GRCh38
NC_000010.10:g.104596802_104596803del , CM000672.1:g.104596802_104596803del GRCh37
NC_000010.9:g.104586792_104586793del NCBI36
NG_007955.1:g.5489_5490del

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.297+20_297+21del MANE Select ENSP00000358903.3:n.297+20_297+21del
ENST00000638190.1:c.297+20_297+21del ENSP00000492539.1:n.297+20_297+21del
ENST00000638272.1:c.297+20_297+21del ENSP00000491508.1:n.297+20_297+21del
ENST00000638971.1:c.297+20_297+21del ENSP00000492313.1:n.297+20_297+21del
ENST00000639393.1:c.297+20_297+21del ENSP00000492651.1:n.297+20_297+21del
ENST00000369887.3:c.297+20_297+21del ENSP00000358903.3:n.297+20_297+21del
ENST00000489268.1:n.350+20_350+21del
NM_000102.3:c.297+20_297+21del NP_000093.1:n.297+20_297+21del
NM_000102.4:c.297+20_297+21del MANE Select NP_000093.1:n.297+20_297+21del
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