Canonical Allele Identifier: CA10634800
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 298615
ClinVar RCV Id: RCV000285334
dbSNP Id: rs45455494
gnomAD v2: 10-104590293-G-GA
gnomAD v3: 10-102830536-G-GA
gnomAD v4: 10-102830536-G-GA
MyVariant Identifiers: chr10:g.104590294dupA (hg19) chr10:g.104590294_104590295insA (hg19) chr10:g.104590293_104590294insA (hg19) chr10:g.102830537dupA (hg38) chr10:g.102830537_102830538insA (hg38) chr10:g.102830536_102830537insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102830547dup , CM000672.2:g.102830547dup GRCh38
NC_000010.10:g.104590304dup , CM000672.1:g.104590304dup GRCh37
NC_000010.9:g.104580294dup NCBI36
NG_007955.1:g.11997dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.*165dup (CYP17A1) MANE Select ENSP00000358903.3:n.*165dup
ENST00000638190.1:c.*165dup (CYP17A1) ENSP00000492539.1:n.*165dup
ENST00000638971.1:c.*165dup (CYP17A1) ENSP00000492313.1:n.*165dup
ENST00000647664.1:c.*418-189dup (WBP1L) ENSP00000498131.1:n.*418-189dup
ENST00000369887.3:c.*165dup (CYP17A1) ENSP00000358903.3:n.*165dup
NM_000102.3:c.*165dup (CYP17A1) NP_000093.1:n.*165dup
NM_000102.4:c.*165dup (CYP17A1) MANE Select NP_000093.1:n.*165dup
Search 100 bp 5'
Search 100 bp 3'