Canonical Allele Identifier: CA377938971
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102832661T>C , CM000672.2:g.102832661T>C GRCh38
NC_000010.10:g.104592418T>C , CM000672.1:g.104592418T>C GRCh37
NC_000010.9:g.104582408T>C NCBI36
NG_007955.1:g.9873A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369887.4:c.989A>G (CYP17A1) MANE Select ENSP00000358903.3:p.Glu330Gly
ENST00000638190.1:c.686A>G (CYP17A1) ENSP00000492539.1:p.Glu229Gly
ENST00000638272.1:c.533A>G (CYP17A1) ENSP00000491508.1:p.Glu178Gly
ENST00000638971.1:c.902A>G (CYP17A1) ENSP00000492313.1:p.Glu301Gly
ENST00000639393.1:c.989A>G (CYP17A1) ENSP00000492651.1:p.Glu330Gly
ENST00000640633.1:n.751A>G (CYP17A1)
ENST00000647664.1:c.*1692T>C (WBP1L) ENSP00000498131.1:n.*1692T>C
ENST00000369887.3:c.989A>G (CYP17A1) ENSP00000358903.3:p.Glu330Gly
NM_000102.3:c.989A>G (CYP17A1) NP_000093.1:p.Glu330Gly
NM_000102.4:c.989A>G (CYP17A1) MANE Select NP_000093.1:p.Glu330Gly