Canonical Allele Identifier: CA115205
Gene: CYP17A1 HGNC NCBI
WBP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1806
ClinVar RCV Id: RCV000001879
dbSNP Id: rs104894151

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102830871A>G , CM000672.2:g.102830871A>G GRCh38
NC_000010.10:g.104590628A>G , CM000672.1:g.104590628A>G GRCh37
NC_000010.9:g.104580618A>G NCBI36
NG_007955.1:g.11663T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369887.4:c.1358T>C (CYP17A1) MANE Select ENSP00000358903.3:p.Phe453Ser
ENST00000638190.1:c.1055T>C (CYP17A1) ENSP00000492539.1:p.Phe352Ser
ENST00000638272.1:c.902T>C (CYP17A1) ENSP00000491508.1:p.Phe301Ser
ENST00000638971.1:c.1271T>C (CYP17A1) ENSP00000492313.1:p.Phe424Ser
ENST00000639393.1:c.1361T>C (CYP17A1) ENSP00000492651.1:p.Phe454Ser
ENST00000640633.1:n.1120T>C (CYP17A1)
ENST00000647664.1:c.*553A>G (WBP1L) ENSP00000498131.1:n.*553A>G
ENST00000369887.3:c.1358T>C (CYP17A1) ENSP00000358903.3:p.Phe453Ser
NM_000102.3:c.1358T>C (CYP17A1) NP_000093.1:p.Phe453Ser
NM_000102.4:c.1358T>C (CYP17A1) MANE Select NP_000093.1:p.Phe453Ser