Canonical Allele Identifier: CA357502243
Gene: MTTP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99583446T>C , CM000666.2:g.99583446T>C GRCh38
NC_000004.11:g.100504603T>C , CM000666.1:g.100504603T>C GRCh37
NC_000004.10:g.100723626T>C NCBI36
NG_011469.1:g.24364T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265517.10:c.322T>C MANE Select ENSP00000265517.5:p.Ser108Pro
ENST00000457717.6:c.322T>C ENSP00000400821.1:p.Ser108Pro
ENST00000511045.6:c.73T>C ENSP00000427679.2:p.Ser25Pro
ENST00000265517.9:c.322T>C ENSP00000265517.5:p.Ser108Pro
ENST00000422897.6:c.322T>C ENSP00000407350.2:p.Ser108Pro
ENST00000457717.5:c.322T>C ENSP00000400821.1:p.Ser108Pro
ENST00000506883.5:c.352T>C ENSP00000426755.1:p.Ser118Pro
ENST00000511045.5:c.403T>C ENSP00000427679.1:p.Ser135Pro
ENST00000515141.5:c.*385T>C ENSP00000425642.1:n.*385T>C
ENST00000619629.1:c.322T>C ENSP00000482850.1:p.Ser108Pro
NM_000253.3:c.322T>C NP_000244.2:p.Ser108Pro
NM_001300785.1:c.403T>C NP_001287714.1:p.Ser135Pro
NM_000253.4:c.322T>C NP_000244.2:p.Ser108Pro
NM_001300785.2:c.73T>C NP_001287714.2:p.Ser25Pro
NM_001386140.1:c.322T>C MANE Select NP_001373069.1:p.Ser108Pro