Canonical Allele Identifier: CA471287298

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102830891-G-T
• MyVariant Identifiers: chr10:g.104590648G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830891G>T , CM000672.2:g.102830891G>T	GRCh38
NC_000010.10:g.104590648G>T , CM000672.1:g.104590648G>T	GRCh37
NC_000010.9:g.104580638G>T	NCBI36
NG_007955.1:g.11643C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1338C>A (CYP17A1) MANE Select	ENSP00000358903.3:p.Ile446=
ENST00000638190.1:c.1035C>A (CYP17A1)	ENSP00000492539.1:p.Ile345=
ENST00000638272.1:c.882C>A (CYP17A1)	ENSP00000491508.1:p.Ile294=
ENST00000638971.1:c.1251C>A (CYP17A1)	ENSP00000492313.1:p.Ile417=
ENST00000639393.1:c.1341C>A (CYP17A1)	ENSP00000492651.1:p.Ile447=
ENST00000640633.1:n.1100C>A (CYP17A1)
ENST00000647664.1:c.*573G>T (WBP1L)	ENSP00000498131.1:n.*573G>T
ENST00000369887.3:c.1338C>A (CYP17A1)	ENSP00000358903.3:p.Ile446=
NM_000102.3:c.1338C>A (CYP17A1)	NP_000093.1:p.Ile446=
NM_000102.4:c.1338C>A (CYP17A1) MANE Select	NP_000093.1:p.Ile446=