Canonical Allele Identifier: CA1480066733
Gene: MTTP HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000265517.10:c.322T= MANE Select ENSP00000265517.5:p.Ser108=
ENST00000457717.6:c.322T= ENSP00000400821.1:p.Ser108=
ENST00000511045.6:c.73T= ENSP00000427679.2:p.Ser25=
ENST00000265517.9:c.322T= ENSP00000265517.5:p.Ser108=
ENST00000422897.6:c.322T= ENSP00000407350.2:p.Ser108=
ENST00000457717.5:c.322T= ENSP00000400821.1:p.Ser108=
ENST00000506883.5:c.352T= ENSP00000426755.1:p.Ser118=
ENST00000511045.5:c.403T= ENSP00000427679.1:p.Ser135=
ENST00000515141.5:c.*385T= ENSP00000425642.1:n.*385T=
ENST00000619629.1:c.322T= ENSP00000482850.1:p.Ser108=
NM_000253.3:c.322T= NP_000244.2:p.Ser108=
NM_001300785.1:c.403T= NP_001287714.1:p.Ser135=
NM_000253.4:c.322T= NP_000244.2:p.Ser108=
NM_001300785.2:c.73T= NP_001287714.2:p.Ser25=
NM_001386140.1:c.322T= MANE Select NP_001373069.1:p.Ser108=