Canonical Allele Identifier: CA649312898
Gene: MTTP HGNC NCBI

Linked Data

COSMIC: COSN15343980
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99622926_99622927insC , CM000666.2:g.99622926_99622927insC GRCh38
NC_000004.11:g.100544083_100544084insC , CM000666.1:g.100544083_100544084insC GRCh37
NC_000004.10:g.100763106_100763107insC NCBI36
NG_011469.1:g.63844_63845insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265517.10:c.*78_*79insC MANE Select ENSP00000265517.5:n.*78_*79insC
ENST00000457717.6:c.*78_*79insC ENSP00000400821.1:n.*78_*79insC
ENST00000511045.6:c.*78_*79insC ENSP00000427679.2:n.*78_*79insC
ENST00000265517.9:c.*78_*79insC ENSP00000265517.5:n.*78_*79insC
ENST00000457717.5:c.*78_*79insC ENSP00000400821.1:n.*78_*79insC
ENST00000511045.5:c.*78_*79insC ENSP00000427679.1:n.*78_*79insC
ENST00000619629.1:c.*1210_*1211insC ENSP00000482850.1:n.*1210_*1211insC
NM_000253.3:c.*78_*79insC NP_000244.2:n.*78_*79insC
NM_001300785.1:c.*78_*79insC NP_001287714.1:n.*78_*79insC
NM_000253.4:c.*78_*79insC NP_000244.2:n.*78_*79insC
NM_001300785.2:c.*78_*79insC NP_001287714.2:n.*78_*79insC
NM_001386140.1:c.*78_*79insC MANE Select NP_001373069.1:n.*78_*79insC
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