Canonical Allele Identifier: CA357502110
Gene: MTTP HGNC NCBI

Linked Data

dbSNP Id: rs1560614633

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99583417A>C , CM000666.2:g.99583417A>C GRCh38
NC_000004.11:g.100504574A>C , CM000666.1:g.100504574A>C GRCh37
NC_000004.10:g.100723597A>C NCBI36
NG_011469.1:g.24335A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000265517.10:c.293A>C MANE Select ENSP00000265517.5:p.Glu98Ala
ENST00000457717.6:c.293A>C ENSP00000400821.1:p.Glu98Ala
ENST00000505094.6:c.44A>C ENSP00000422782.2:p.Glu15Ala
ENST00000511045.6:c.44A>C ENSP00000427679.2:p.Glu15Ala
ENST00000265517.9:c.293A>C ENSP00000265517.5:p.Glu98Ala
ENST00000422897.6:c.293A>C ENSP00000407350.2:p.Glu98Ala
ENST00000457717.5:c.293A>C ENSP00000400821.1:p.Glu98Ala
ENST00000505094.5:c.*383A>C ENSP00000422782.1:n.*383A>C
ENST00000506883.5:c.323A>C ENSP00000426755.1:p.Glu108Ala
ENST00000511045.5:c.374A>C ENSP00000427679.1:p.Glu125Ala
ENST00000515141.5:c.*356A>C ENSP00000425642.1:n.*356A>C
ENST00000619629.1:c.293A>C ENSP00000482850.1:p.Glu98Ala
NM_000253.3:c.293A>C NP_000244.2:p.Glu98Ala
NM_001300785.1:c.374A>C NP_001287714.1:p.Glu125Ala
NM_000253.4:c.293A>C NP_000244.2:p.Glu98Ala
NM_001300785.2:c.44A>C NP_001287714.2:p.Glu15Ala
NM_001386140.1:c.293A>C MANE Select NP_001373069.1:p.Glu98Ala