Canonical Allele Identifier: CA2610720969

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102830988-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102830988G>A , CM000672.2:g.102830988G>A	GRCh38
NC_000010.10:g.104590745G>A , CM000672.1:g.104590745G>A	GRCh37
NC_000010.9:g.104580735G>A	NCBI36
NG_007955.1:g.11546C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1244-3C>T (CYP17A1) MANE Select	ENSP00000358903.3:n.1244-3C>T
ENST00000638190.1:c.941-3C>T (CYP17A1)	ENSP00000492539.1:n.941-3C>T
ENST00000638272.1:c.788-3C>T (CYP17A1)	ENSP00000491508.1:n.788-3C>T
ENST00000638971.1:c.1157-3C>T (CYP17A1)	ENSP00000492313.1:n.1157-3C>T
ENST00000639393.1:c.1247-3C>T (CYP17A1)	ENSP00000492651.1:n.1247-3C>T
ENST00000640633.1:n.1006-3C>T (CYP17A1)
ENST00000647664.1:c.*628+42G>A (WBP1L)	ENSP00000498131.1:n.*628+42G>A
ENST00000369887.3:c.1244-3C>T (CYP17A1)	ENSP00000358903.3:n.1244-3C>T
ENST00000469683.1:n.197-3C>T (CYP17A1)
NM_000102.3:c.1244-3C>T (CYP17A1)	NP_000093.1:n.1244-3C>T
NM_000102.4:c.1244-3C>T (CYP17A1) MANE Select	NP_000093.1:n.1244-3C>T