Canonical Allele Identifier: CA471287469
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

gnomAD v4: 10-102830969-T-C
MyVariant Identifiers: chr10:g.104590726T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102830969T>C , CM000672.2:g.102830969T>C GRCh38
NC_000010.10:g.104590726T>C , CM000672.1:g.104590726T>C GRCh37
NC_000010.9:g.104580716T>C NCBI36
NG_007955.1:g.11565A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.1260A>G (CYP17A1) MANE Select ENSP00000358903.3:p.Pro420=
ENST00000638190.1:c.957A>G (CYP17A1) ENSP00000492539.1:p.Pro319=
ENST00000638272.1:c.804A>G (CYP17A1) ENSP00000491508.1:p.Pro268=
ENST00000638971.1:c.1173A>G (CYP17A1) ENSP00000492313.1:p.Pro391=
ENST00000639393.1:c.1263A>G (CYP17A1) ENSP00000492651.1:p.Pro421=
ENST00000640633.1:n.1022A>G (CYP17A1)
ENST00000647664.1:c.*628+23T>C (WBP1L) ENSP00000498131.1:n.*628+23T>C
ENST00000369887.3:c.1260A>G (CYP17A1) ENSP00000358903.3:p.Pro420=
ENST00000469683.1:n.213A>G (CYP17A1)
NM_000102.3:c.1260A>G (CYP17A1) NP_000093.1:p.Pro420=
NM_000102.4:c.1260A>G (CYP17A1) MANE Select NP_000093.1:p.Pro420=
Search 100 bp 5'
Search 100 bp 3'