Canonical Allele Identifier: CA377938835
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832601A>C , CM000672.2:g.102832601A>C GRCh38
NC_000010.10:g.104592358A>C , CM000672.1:g.104592358A>C GRCh37
NC_000010.9:g.104582348A>C NCBI36
NG_007955.1:g.9933T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.1049T>G (CYP17A1) MANE Select ENSP00000358903.3:p.Leu350Arg
ENST00000638190.1:c.746T>G (CYP17A1) ENSP00000492539.1:p.Leu249Arg
ENST00000638272.1:c.593T>G (CYP17A1) ENSP00000491508.1:p.Leu198Arg
ENST00000638971.1:c.962T>G (CYP17A1) ENSP00000492313.1:p.Leu321Arg
ENST00000639393.1:c.1049T>G (CYP17A1) ENSP00000492651.1:p.Leu350Arg
ENST00000640633.1:n.811T>G (CYP17A1)
ENST00000647664.1:c.*1632A>C (WBP1L) ENSP00000498131.1:n.*1632A>C
ENST00000369887.3:c.1049T>G (CYP17A1) ENSP00000358903.3:p.Leu350Arg
NM_000102.3:c.1049T>G (CYP17A1) NP_000093.1:p.Leu350Arg
NM_000102.4:c.1049T>G (CYP17A1) MANE Select NP_000093.1:p.Leu350Arg