Canonical Allele Identifier: CA212782
Gene: CYP17A1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1795
ClinVar RCV Id: RCV000001868
dbSNP Id: rs786205062

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837134_102837158del , CM000672.2:g.102837134_102837158del GRCh38
NC_000010.10:g.104596891_104596915del , CM000672.1:g.104596891_104596915del GRCh37
NC_000010.9:g.104586881_104586905del NCBI36
NG_007955.1:g.5378_5402del

Transcript Alleles

HGVS Amino-acid change
NM_000102.3:c.206_230del VV NP_000093.1:p.Gly69AlafsTer26
NM_000102.4:c.206_230del VV MANE Preferred NP_000093.1:p.Gly69AlafsTer26
ENST00000369887.3:c.206_230del ENSP00000358903.3:p.Gly69AlafsTer26
ENST00000489268.1:n.259_283del