Canonical Allele Identifier: CA659056150

Gene: CYP17A1 WBP1L

Linked Data

• dbSNP Id: rs1426280350
• gnomAD v4: 10-102831369-T-A
• MyVariant Identifiers: chr10:g.104591126T>A (hg19) ; chr10:g.102831369T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831369T>A , CM000672.2:g.102831369T>A	GRCh38
NC_000010.10:g.104591126T>A , CM000672.1:g.104591126T>A	GRCh37
NC_000010.9:g.104581116T>A	NCBI36
NG_007955.1:g.11165A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369887.4:c.1243+139A>T (CYP17A1) MANE Select	ENSP00000358903.3:n.1243+139A>T
ENST00000638190.1:c.940+139A>T (CYP17A1)	ENSP00000492539.1:n.940+139A>T
ENST00000638272.1:c.787+139A>T (CYP17A1)	ENSP00000491508.1:n.787+139A>T
ENST00000638971.1:c.1156+139A>T (CYP17A1)	ENSP00000492313.1:n.1156+139A>T
ENST00000639393.1:c.1246+139A>T (CYP17A1)	ENSP00000492651.1:n.1246+139A>T
ENST00000640633.1:n.1005+139A>T (CYP17A1)
ENST00000647664.1:c.*629-229T>A (WBP1L)	ENSP00000498131.1:n.*629-229T>A
ENST00000369887.3:c.1243+139A>T (CYP17A1)	ENSP00000358903.3:n.1243+139A>T
ENST00000469683.1:n.196+139A>T (CYP17A1)
NM_000102.3:c.1243+139A>T (CYP17A1)	NP_000093.1:n.1243+139A>T
NM_000102.4:c.1243+139A>T (CYP17A1) MANE Select	NP_000093.1:n.1243+139A>T