Canonical Allele Identifier: CA2610721712

Gene: CYP17A1 WBP1L

Linked Data

• gnomAD v4: 10-102831442-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102831442A>G , CM000672.2:g.102831442A>G	GRCh38
NC_000010.10:g.104591199A>G , CM000672.1:g.104591199A>G	GRCh37
NC_000010.9:g.104581189A>G	NCBI36
NG_007955.1:g.11092T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369887.4:c.1243+66T>C (CYP17A1) MANE Select	ENSP00000358903.3:n.1243+66T>C
ENST00000638190.1:c.940+66T>C (CYP17A1)	ENSP00000492539.1:n.940+66T>C
ENST00000638272.1:c.787+66T>C (CYP17A1)	ENSP00000491508.1:n.787+66T>C
ENST00000638971.1:c.1156+66T>C (CYP17A1)	ENSP00000492313.1:n.1156+66T>C
ENST00000639393.1:c.1246+66T>C (CYP17A1)	ENSP00000492651.1:n.1246+66T>C
ENST00000640633.1:n.1005+66T>C (CYP17A1)
ENST00000647664.1:c.*629-156A>G (WBP1L)	ENSP00000498131.1:n.*629-156A>G
ENST00000369887.3:c.1243+66T>C (CYP17A1)	ENSP00000358903.3:n.1243+66T>C
ENST00000469683.1:n.196+66T>C (CYP17A1)
NM_000102.3:c.1243+66T>C (CYP17A1)	NP_000093.1:n.1243+66T>C
NM_000102.4:c.1243+66T>C (CYP17A1) MANE Select	NP_000093.1:n.1243+66T>C