Canonical Allele Identifier: CA5669563
Gene: CYP17A1 HGNC NCBI

Linked Data

dbSNP Id: rs746879000
ExAC: 10:104594823 CT / C
gnomAD v2: 10-104594823-CT-C
gnomAD v4: 10-102835066-CT-C
MyVariant Identifiers: chr10:g.104594824del (hg19) chr10:g.102835067del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102835067del , CM000672.2:g.102835067del GRCh38
NC_000010.10:g.104594824del , CM000672.1:g.104594824del GRCh37
NC_000010.9:g.104584814del NCBI36
NG_007955.1:g.7467del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.437-53del MANE Select ENSP00000358903.3:n.437-53del
ENST00000638190.1:c.437-53del ENSP00000492539.1:n.437-53del
ENST00000638272.1:c.298-1859del ENSP00000491508.1:n.298-1859del
ENST00000638971.1:c.437-53del ENSP00000492313.1:n.437-53del
ENST00000639393.1:c.437-53del ENSP00000492651.1:n.437-53del
ENST00000640633.1:n.199-53del
ENST00000369887.3:c.437-53del ENSP00000358903.3:n.437-53del
ENST00000489268.1:n.691-53del
NM_000102.3:c.437-53del NP_000093.1:n.437-53del
NM_000102.4:c.437-53del MANE Select NP_000093.1:n.437-53del
Search 100 bp 5'
Search 100 bp 3'