Canonical Allele Identifier: CA2695203670

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99622774del , CM000666.2:g.99622774del	GRCh38
NC_000004.11:g.100543931del , CM000666.1:g.100543931del	GRCh37
NC_000004.10:g.100762954del	NCBI36
NG_011469.1:g.63692del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.2611del MANE Select	ENSP00000265517.5:p.His871IlefsTer29
ENST00000457717.6:c.2611del	ENSP00000400821.1:p.His871IlefsTer29
ENST00000511045.6:c.2362del	ENSP00000427679.2:p.His788IlefsTer29
ENST00000265517.9:c.2611del	ENSP00000265517.5:p.His871IlefsTer29
ENST00000457717.5:c.2611del	ENSP00000400821.1:p.His871IlefsTer29
ENST00000511045.5:c.2692del	ENSP00000427679.1:p.His898IlefsTer29
ENST00000619629.1:c.*1058del	ENSP00000482850.1:n.*1058del
NM_000253.3:c.2611del	NP_000244.2:p.His871IlefsTer29
NM_001300785.1:c.2692del	NP_001287714.1:p.His898IlefsTer29
NM_000253.4:c.2611del	NP_000244.2:p.His871IlefsTer29
NM_001300785.2:c.2362del	NP_001287714.2:p.His788IlefsTer29
NM_001386140.1:c.2611del MANE Select	NP_001373069.1:p.His871IlefsTer29