Canonical Allele Identifier: CA2610723989

Gene: CYP17A1 CYP17A1-AS1

Linked Data

• gnomAD v4: 10-102834062-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102834063del , CM000672.2:g.102834063del	GRCh38
NC_000010.10:g.104593820del , CM000672.1:g.104593820del	GRCh37
NC_000010.9:g.104583810del	NCBI36
NG_007955.1:g.8471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369884.4:n.152-114del
ENST00000369887.4:c.726del (CYP17A1) MANE Select	ENSP00000358903.3:p.Leu243Ter
ENST00000638190.1:c.666+722del (CYP17A1)	ENSP00000492539.1:n.666+722del
ENST00000638272.1:c.298-855del (CYP17A1)	ENSP00000491508.1:n.298-855del
ENST00000638971.1:c.666+722del (CYP17A1)	ENSP00000492313.1:n.666+722del
ENST00000639393.1:c.726del (CYP17A1)	ENSP00000492651.1:p.Leu243Ter
ENST00000640633.1:n.488del (CYP17A1)
ENST00000369887.3:c.726del (CYP17A1)	ENSP00000358903.3:p.Leu243Ter
ENST00000489268.1:n.1642del (CYP17A1)
NM_000102.3:c.726del (CYP17A1)	NP_000093.1:p.Leu243Ter
XR_428804.1:n.206-114del (CYP17A1-AS1)
NM_000102.4:c.726del (CYP17A1) MANE Select	NP_000093.1:p.Leu243Ter