Canonical Allele Identifier: CA377938250
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104590677C>G (hg19) chr10:g.102830920C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102830920C>G , CM000672.2:g.102830920C>G GRCh38
NC_000010.10:g.104590677C>G , CM000672.1:g.104590677C>G GRCh37
NC_000010.9:g.104580667C>G NCBI36
NG_007955.1:g.11614G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.1309G>C (CYP17A1) MANE Select ENSP00000358903.3:p.Ala437Pro
ENST00000638190.1:c.1006G>C (CYP17A1) ENSP00000492539.1:p.Ala336Pro
ENST00000638272.1:c.853G>C (CYP17A1) ENSP00000491508.1:p.Ala285Pro
ENST00000638971.1:c.1222G>C (CYP17A1) ENSP00000492313.1:p.Ala408Pro
ENST00000639393.1:c.1312G>C (CYP17A1) ENSP00000492651.1:p.Ala438Pro
ENST00000640633.1:n.1071G>C (CYP17A1)
ENST00000647664.1:c.*602C>G (WBP1L) ENSP00000498131.1:n.*602C>G
ENST00000369887.3:c.1309G>C (CYP17A1) ENSP00000358903.3:p.Ala437Pro
NM_000102.3:c.1309G>C (CYP17A1) NP_000093.1:p.Ala437Pro
NM_000102.4:c.1309G>C (CYP17A1) MANE Select NP_000093.1:p.Ala437Pro
Search 100 bp 5'
Search 100 bp 3'