Canonical Allele Identifier: CA357509546
Community Standard Title: NM_001386140.1(MTTP):c.1321C>T (p.Gln441Ter)
Gene: MTTP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99601691C>T , CM000666.2:g.99601691C>T GRCh38
NC_000004.11:g.100522848C>T , CM000666.1:g.100522848C>T GRCh37
NC_000004.10:g.100741871C>T NCBI36
NG_011469.1:g.42609C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001386140.1:c.1321C>T MANE Select NP_001373069.1:p.Gln441Ter
ENST00000265517.10:c.1321C>T MANE Select ENSP00000265517.5:p.Gln441Ter
NM_000253.3:c.1321C>T NP_000244.2:p.Gln441Ter
NM_000253.4:c.1321C>T NP_000244.2:p.Gln441Ter
NM_001300785.1:c.1402C>T NP_001287714.1:p.Gln468Ter
NM_001300785.2:c.1072C>T NP_001287714.2:p.Gln358Ter
ENST00000265517.9:c.1321C>T ENSP00000265517.5:p.Gln441Ter
ENST00000457717.5:c.1321C>T ENSP00000400821.1:p.Gln441Ter
ENST00000457717.6:c.1321C>T ENSP00000400821.1:p.Gln441Ter
ENST00000511045.5:c.1402C>T ENSP00000427679.1:p.Gln468Ter
ENST00000511045.6:c.1072C>T ENSP00000427679.2:p.Gln358Ter
ENST00000619629.1:c.1321C>T ENSP00000482850.1:p.Gln441Ter