Canonical Allele Identifier: CA471287321

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102830906-G-A
• MyVariant Identifiers: chr10:g.104590663G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830906G>A , CM000672.2:g.102830906G>A	GRCh38
NC_000010.10:g.104590663G>A , CM000672.1:g.104590663G>A	GRCh37
NC_000010.9:g.104580653G>A	NCBI36
NG_007955.1:g.11628C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1323C>T (CYP17A1) MANE Select	ENSP00000358903.3:p.Ser441=
ENST00000638190.1:c.1020C>T (CYP17A1)	ENSP00000492539.1:p.Ser340=
ENST00000638272.1:c.867C>T (CYP17A1)	ENSP00000491508.1:p.Ser289=
ENST00000638971.1:c.1236C>T (CYP17A1)	ENSP00000492313.1:p.Ser412=
ENST00000639393.1:c.1326C>T (CYP17A1)	ENSP00000492651.1:p.Ser442=
ENST00000640633.1:n.1085C>T (CYP17A1)
ENST00000647664.1:c.*588G>A (WBP1L)	ENSP00000498131.1:n.*588G>A
ENST00000369887.3:c.1323C>T (CYP17A1)	ENSP00000358903.3:p.Ser441=
NM_000102.3:c.1323C>T (CYP17A1)	NP_000093.1:p.Ser441=
NM_000102.4:c.1323C>T (CYP17A1) MANE Select	NP_000093.1:p.Ser441=