Canonical Allele Identifier: CA2610721011

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102831001-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831001G>T , CM000672.2:g.102831001G>T	GRCh38
NC_000010.10:g.104590758G>T , CM000672.1:g.104590758G>T	GRCh37
NC_000010.9:g.104580748G>T	NCBI36
NG_007955.1:g.11533C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1244-16C>A (CYP17A1) MANE Select	ENSP00000358903.3:n.1244-16C>A
ENST00000638190.1:c.941-16C>A (CYP17A1)	ENSP00000492539.1:n.941-16C>A
ENST00000638272.1:c.788-16C>A (CYP17A1)	ENSP00000491508.1:n.788-16C>A
ENST00000638971.1:c.1157-16C>A (CYP17A1)	ENSP00000492313.1:n.1157-16C>A
ENST00000639393.1:c.1247-16C>A (CYP17A1)	ENSP00000492651.1:n.1247-16C>A
ENST00000640633.1:n.1006-16C>A (CYP17A1)
ENST00000647664.1:c.*628+55G>T (WBP1L)	ENSP00000498131.1:n.*628+55G>T
ENST00000369887.3:c.1244-16C>A (CYP17A1)	ENSP00000358903.3:n.1244-16C>A
ENST00000469683.1:n.197-16C>A (CYP17A1)
NM_000102.3:c.1244-16C>A (CYP17A1)	NP_000093.1:n.1244-16C>A
NM_000102.4:c.1244-16C>A (CYP17A1) MANE Select	NP_000093.1:n.1244-16C>A