Canonical Allele Identifier: CA377938342

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102830964-C-A
• MyVariant Identifiers: chr10:g.104590721C>A (hg19) ; chr10:g.102830964C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830964C>A , CM000672.2:g.102830964C>A	GRCh38
NC_000010.10:g.104590721C>A , CM000672.1:g.104590721C>A	GRCh37
NC_000010.9:g.104580711C>A	NCBI36
NG_007955.1:g.11570G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1265G>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Gly422Val
ENST00000638190.1:c.962G>T (CYP17A1)	ENSP00000492539.1:p.Gly321Val
ENST00000638272.1:c.809G>T (CYP17A1)	ENSP00000491508.1:p.Gly270Val
ENST00000638971.1:c.1178G>T (CYP17A1)	ENSP00000492313.1:p.Gly393Val
ENST00000639393.1:c.1268G>T (CYP17A1)	ENSP00000492651.1:p.Gly423Val
ENST00000640633.1:n.1027G>T (CYP17A1)
ENST00000647664.1:c.*628+18C>A (WBP1L)	ENSP00000498131.1:n.*628+18C>A
ENST00000369887.3:c.1265G>T (CYP17A1)	ENSP00000358903.3:p.Gly422Val
ENST00000469683.1:n.218G>T (CYP17A1)
NM_000102.3:c.1265G>T (CYP17A1)	NP_000093.1:p.Gly422Val
NM_000102.4:c.1265G>T (CYP17A1) MANE Select	NP_000093.1:p.Gly422Val