Canonical Allele Identifier: CA2580071915
Community Standard Title: NM_001386140.1(MTTP):c.1168del (p.Gln390ArgfsTer19)
Gene: MTTP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99600665del , CM000666.2:g.99600665del GRCh38
NC_000004.11:g.100521822del , CM000666.1:g.100521822del GRCh37
NC_000004.10:g.100740845del NCBI36
NG_011469.1:g.41583del

Transcript Alleles

HGVS Amino-acid Change
NM_001386140.1:c.1168del MANE Select NP_001373069.1:p.Gln390ArgfsTer19
ENST00000265517.10:c.1168del MANE Select ENSP00000265517.5:p.Gln390ArgfsTer19
NM_000253.3:c.1168del NP_000244.2:p.Gln390ArgfsTer19
NM_000253.4:c.1168del NP_000244.2:p.Gln390ArgfsTer19
NM_001300785.1:c.1249del NP_001287714.1:p.Gln417ArgfsTer19
NM_001300785.2:c.919del NP_001287714.2:p.Gln307ArgfsTer19
ENST00000265517.9:c.1168del ENSP00000265517.5:p.Gln390ArgfsTer19
ENST00000457717.5:c.1168del ENSP00000400821.1:p.Gln390ArgfsTer19
ENST00000457717.6:c.1168del ENSP00000400821.1:p.Gln390ArgfsTer19
ENST00000511045.5:c.1249del ENSP00000427679.1:p.Gln417ArgfsTer19
ENST00000511045.6:c.919del ENSP00000427679.2:p.Gln307ArgfsTer19
ENST00000619629.1:c.1168del ENSP00000482850.1:p.Gln390ArgfsTer19