Canonical Allele Identifier: CA2574686178
Gene: CYP17A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835209_102835212del , CM000672.2:g.102835209_102835212del GRCh38
NC_000010.10:g.104594966_104594969del , CM000672.1:g.104594966_104594969del GRCh37
NC_000010.9:g.104584956_104584959del NCBI36
NG_007955.1:g.7322_7325del

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.436+42_436+45del MANE Select ENSP00000358903.3:n.436+42_436+45del
ENST00000638190.1:c.436+42_436+45del ENSP00000492539.1:n.436+42_436+45del
ENST00000638272.1:c.297+1853_297+1856del ENSP00000491508.1:n.297+1853_297+1856del
ENST00000638971.1:c.436+42_436+45del ENSP00000492313.1:n.436+42_436+45del
ENST00000639393.1:c.436+42_436+45del ENSP00000492651.1:n.436+42_436+45del
ENST00000640633.1:n.198+42_198+45del
ENST00000369887.3:c.436+42_436+45del ENSP00000358903.3:n.436+42_436+45del
ENST00000489268.1:n.690+42_690+45del
NM_000102.3:c.436+42_436+45del NP_000093.1:n.436+42_436+45del
NM_000102.4:c.436+42_436+45del MANE Select NP_000093.1:n.436+42_436+45del
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