Canonical Allele Identifier: CA357520891
Gene: MTTP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99622844T>G , CM000666.2:g.99622844T>G GRCh38
NC_000004.11:g.100544001T>G , CM000666.1:g.100544001T>G GRCh37
NC_000004.10:g.100763024T>G NCBI36
NG_011469.1:g.63762T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265517.10:c.2681T>G MANE Select ENSP00000265517.5:p.Phe894Cys
ENST00000457717.6:c.2681T>G ENSP00000400821.1:p.Phe894Cys
ENST00000511045.6:c.2432T>G ENSP00000427679.2:p.Phe811Cys
ENST00000265517.9:c.2681T>G ENSP00000265517.5:p.Phe894Cys
ENST00000457717.5:c.2681T>G ENSP00000400821.1:p.Phe894Cys
ENST00000511045.5:c.2762T>G ENSP00000427679.1:p.Phe921Cys
ENST00000619629.1:c.*1128T>G ENSP00000482850.1:n.*1128T>G
NM_000253.3:c.2681T>G NP_000244.2:p.Phe894Cys
NM_001300785.1:c.2762T>G NP_001287714.1:p.Phe921Cys
NM_000253.4:c.2681T>G NP_000244.2:p.Phe894Cys
NM_001300785.2:c.2432T>G NP_001287714.2:p.Phe811Cys
NM_001386140.1:c.2681T>G MANE Select NP_001373069.1:p.Phe894Cys