Canonical Allele Identifier: CA2559501117
Gene: MTTP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99622920C>T , CM000666.2:g.99622920C>T GRCh38
NC_000004.11:g.100544077C>T , CM000666.1:g.100544077C>T GRCh37
NC_000004.10:g.100763100C>T NCBI36
NG_011469.1:g.63838C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265517.10:c.*72C>T MANE Select ENSP00000265517.5:n.*72C>T
ENST00000457717.6:c.*72C>T ENSP00000400821.1:n.*72C>T
ENST00000511045.6:c.*72C>T ENSP00000427679.2:n.*72C>T
ENST00000265517.9:c.*72C>T ENSP00000265517.5:n.*72C>T
ENST00000457717.5:c.*72C>T ENSP00000400821.1:n.*72C>T
ENST00000511045.5:c.*72C>T ENSP00000427679.1:n.*72C>T
ENST00000619629.1:c.*1204C>T ENSP00000482850.1:n.*1204C>T
NM_000253.3:c.*72C>T NP_000244.2:n.*72C>T
NM_001300785.1:c.*72C>T NP_001287714.1:n.*72C>T
NM_000253.4:c.*72C>T NP_000244.2:n.*72C>T
NM_001300785.2:c.*72C>T NP_001287714.2:n.*72C>T
NM_001386140.1:c.*72C>T MANE Select NP_001373069.1:n.*72C>T