Canonical Allele Identifier: CA377938827
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.104592353G>C (hg19) chr10:g.102832596G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832596G>C , CM000672.2:g.102832596G>C GRCh38
NC_000010.10:g.104592353G>C , CM000672.1:g.104592353G>C GRCh37
NC_000010.9:g.104582343G>C NCBI36
NG_007955.1:g.9938C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.1054C>G (CYP17A1) MANE Select ENSP00000358903.3:p.Leu352Val
ENST00000638190.1:c.751C>G (CYP17A1) ENSP00000492539.1:p.Leu251Val
ENST00000638272.1:c.598C>G (CYP17A1) ENSP00000491508.1:p.Leu200Val
ENST00000638971.1:c.967C>G (CYP17A1) ENSP00000492313.1:p.Leu323Val
ENST00000639393.1:c.1054C>G (CYP17A1) ENSP00000492651.1:p.Leu352Val
ENST00000640633.1:n.816C>G (CYP17A1)
ENST00000647664.1:c.*1627G>C (WBP1L) ENSP00000498131.1:n.*1627G>C
ENST00000369887.3:c.1054C>G (CYP17A1) ENSP00000358903.3:p.Leu352Val
NM_000102.3:c.1054C>G (CYP17A1) NP_000093.1:p.Leu352Val
NM_000102.4:c.1054C>G (CYP17A1) MANE Select NP_000093.1:p.Leu352Val
Search 100 bp 5'
Search 100 bp 3'