Canonical Allele Identifier: CA645520133

Gene: MTTP

Linked Data

• COSMIC: COSM5691462

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622749_99622772del , CM000666.2:g.99622749_99622772del	GRCh38
NC_000004.11:g.100543906_100543929del , CM000666.1:g.100543906_100543929del	GRCh37
NC_000004.10:g.100762929_100762952del	NCBI36
NG_011469.1:g.63667_63690del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265517.10:c.2586_2609del MANE Select	ENSP00000265517.5:p.Leu863_Leu870del
ENST00000457717.6:c.2586_2609del	ENSP00000400821.1:p.Leu863_Leu870del
ENST00000511045.6:c.2337_2360del	ENSP00000427679.2:p.Leu780_Leu787del
ENST00000265517.9:c.2586_2609del	ENSP00000265517.5:p.Leu863_Leu870del
ENST00000457717.5:c.2586_2609del	ENSP00000400821.1:p.Leu863_Leu870del
ENST00000511045.5:c.2667_2690del	ENSP00000427679.1:p.Leu890_Leu897del
ENST00000619629.1:c.*1033_*1056del	ENSP00000482850.1:n.*1033_*1056del
NM_000253.3:c.2586_2609del	NP_000244.2:p.Leu863_Leu870del
NM_001300785.1:c.2667_2690del	NP_001287714.1:p.Leu890_Leu897del
NM_000253.4:c.2586_2609del	NP_000244.2:p.Leu863_Leu870del
NM_001300785.2:c.2337_2360del	NP_001287714.2:p.Leu780_Leu787del
NM_001386140.1:c.2586_2609del MANE Select	NP_001373069.1:p.Leu863_Leu870del