Canonical Allele Identifier: CA2322454465

Gene: KEAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10489768_10489784delinsGACGATTGAGGACAGCC , CM000681.2:g.10489768_10489784delinsGACGATTGAGGACAGCC	GRCh38
NC_000019.9:g.10600444_10600460delinsGACGATTGAGGACAGCC , CM000681.1:g.10600444_10600460delinsGACGATTGAGGACAGCC	GRCh37
NC_000019.8:g.10461444_10461460delinsGACGATTGAGGACAGCC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000171111.10:c.1395_1411delinsGGCTGTCCTCAATCGTC MANE Select	ENSP00000171111.4:p.Val465=
ENST00000171111.9:c.1395_1411delinsGGCTGTCCTCAATCGTC	ENSP00000171111.4:p.Val465=
ENST00000393623.6:c.1395_1411delinsGGCTGTCCTCAATCGTC	ENSP00000377245.1:p.Val465=
ENST00000590593.1:c.305-416_305-400delinsGGCTGTCCTCAATCGTC
ENST00000592478.5:c.214_230delinsGGCTGTCCTCAATCGTC
NM_012289.3:c.1395_1411delinsGGCTGTCCTCAATCGTC	NP_036421.2:p.Val465=
NM_203500.1:c.1395_1411delinsGGCTGTCCTCAATCGTC	NP_987096.1:p.Val465=
XM_005260173.1:c.1395_1411delinsGGCTGTCCTCAATCGTC	XP_005260230.1:p.Val465=
XM_005260174.1:c.1395_1411delinsGGCTGTCCTCAATCGTC	XP_005260231.1:p.Val465=
XM_011528452.1:c.1395_1411delinsGGCTGTCCTCAATCGTC	XP_011526754.1:p.Val465=
NM_203500.2:c.1395_1411delinsGGCTGTCCTCAATCGTC MANE Select	NP_987096.1:p.Val465=
NM_012289.4:c.1395_1411delinsGGCTGTCCTCAATCGTC	NP_036421.2:p.Val465=