Canonical Allele Identifier: CA357520681
Gene: MTTP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99622808T>C , CM000666.2:g.99622808T>C GRCh38
NC_000004.11:g.100543965T>C , CM000666.1:g.100543965T>C GRCh37
NC_000004.10:g.100762988T>C NCBI36
NG_011469.1:g.63726T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265517.10:c.2645T>C MANE Select ENSP00000265517.5:p.Phe882Ser
ENST00000457717.6:c.2645T>C ENSP00000400821.1:p.Phe882Ser
ENST00000511045.6:c.2396T>C ENSP00000427679.2:p.Phe799Ser
ENST00000265517.9:c.2645T>C ENSP00000265517.5:p.Phe882Ser
ENST00000457717.5:c.2645T>C ENSP00000400821.1:p.Phe882Ser
ENST00000511045.5:c.2726T>C ENSP00000427679.1:p.Phe909Ser
ENST00000619629.1:c.*1092T>C ENSP00000482850.1:n.*1092T>C
NM_000253.3:c.2645T>C NP_000244.2:p.Phe882Ser
NM_001300785.1:c.2726T>C NP_001287714.1:p.Phe909Ser
NM_000253.4:c.2645T>C NP_000244.2:p.Phe882Ser
NM_001300785.2:c.2396T>C NP_001287714.2:p.Phe799Ser
NM_001386140.1:c.2645T>C MANE Select NP_001373069.1:p.Phe882Ser