Canonical Allele Identifier: CA377938736

Gene: CYP17A1 WBP1L

Linked Data

• MyVariant Identifiers: chr10:g.104592305G>T (hg19) ; chr10:g.102832548G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102832548G>T , CM000672.2:g.102832548G>T	GRCh38
NC_000010.10:g.104592305G>T , CM000672.1:g.104592305G>T	GRCh37
NC_000010.9:g.104582295G>T	NCBI36
NG_007955.1:g.9986C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1102C>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Pro368Thr
ENST00000638190.1:c.799C>A (CYP17A1)	ENSP00000492539.1:p.Pro267Thr
ENST00000638272.1:c.646C>A (CYP17A1)	ENSP00000491508.1:p.Pro216Thr
ENST00000638971.1:c.1015C>A (CYP17A1)	ENSP00000492313.1:p.Pro339Thr
ENST00000639393.1:c.1102C>A (CYP17A1)	ENSP00000492651.1:p.Pro368Thr
ENST00000640633.1:n.864C>A (CYP17A1)
ENST00000647664.1:c.*1579G>T (WBP1L)	ENSP00000498131.1:n.*1579G>T
ENST00000369887.3:c.1102C>A (CYP17A1)	ENSP00000358903.3:p.Pro368Thr
NM_000102.3:c.1102C>A (CYP17A1)	NP_000093.1:p.Pro368Thr
NM_000102.4:c.1102C>A (CYP17A1) MANE Select	NP_000093.1:p.Pro368Thr