Canonical Allele Identifier: CA2574686169
Gene: CYP17A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835169del , CM000672.2:g.102835169del GRCh38
NC_000010.10:g.104594926del , CM000672.1:g.104594926del GRCh37
NC_000010.9:g.104584916del NCBI36
NG_007955.1:g.7366del

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.436+86del MANE Select ENSP00000358903.3:n.436+86del
ENST00000638190.1:c.436+86del ENSP00000492539.1:n.436+86del
ENST00000638272.1:c.297+1897del ENSP00000491508.1:n.297+1897del
ENST00000638971.1:c.436+86del ENSP00000492313.1:n.436+86del
ENST00000639393.1:c.436+86del ENSP00000492651.1:n.436+86del
ENST00000640633.1:n.198+86del
ENST00000369887.3:c.436+86del ENSP00000358903.3:n.436+86del
ENST00000489268.1:n.690+86del
NM_000102.3:c.436+86del NP_000093.1:n.436+86del
NM_000102.4:c.436+86del MANE Select NP_000093.1:n.436+86del
Search 100 bp 5'
Search 100 bp 3'