Canonical Allele Identifier: CA5669371
Community Standard Title: NM_000102.4(CYP17A1):c.1226C>G (p.Pro409Arg)
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102831525G>C , CM000672.2:g.102831525G>C GRCh38
NC_000010.10:g.104591282G>C , CM000672.1:g.104591282G>C GRCh37
NC_000010.9:g.104581272G>C NCBI36
NG_007955.1:g.11009C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000102.4:c.1226C>G (CYP17A1) MANE Select NP_000093.1:p.Pro409Arg
ENST00000369887.4:c.1226C>G (CYP17A1) MANE Select ENSP00000358903.3:p.Pro409Arg
NM_000102.3:c.1226C>G (CYP17A1) NP_000093.1:p.Pro409Arg
ENST00000369887.3:c.1226C>G (CYP17A1) ENSP00000358903.3:p.Pro409Arg
ENST00000469683.1:n.179C>G (CYP17A1)
ENST00000638190.1:c.923C>G (CYP17A1) ENSP00000492539.1:p.Pro308Arg
ENST00000638272.1:c.770C>G (CYP17A1) ENSP00000491508.1:p.Pro257Arg
ENST00000638971.1:c.1139C>G (CYP17A1) ENSP00000492313.1:p.Pro380Arg
ENST00000639393.1:c.1229C>G (CYP17A1) ENSP00000492651.1:p.Pro410Arg
ENST00000640633.1:n.988C>G (CYP17A1)
ENST00000647664.1:c.*629-73G>C (WBP1L) ENSP00000498131.1:n.*629-73G>C