Canonical Allele Identifier: CA1480066767
Gene: MTTP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99583527C= , CM000666.2:g.99583527C= GRCh38
NC_000004.11:g.100504684C= , CM000666.1:g.100504684C= GRCh37
NC_000004.10:g.100723707C= NCBI36
NG_011469.1:g.24445C=

Transcript Alleles

HGVS Amino-acid change
ENST00000265517.10:c.393+10C= MANE Select ENSP00000265517.5:n.393+10C=
ENST00000457717.6:c.393+10C= ENSP00000400821.1:n.393+10C=
ENST00000511045.6:c.144+10C= ENSP00000427679.2:n.144+10C=
ENST00000265517.9:c.393+10C= ENSP00000265517.5:n.393+10C=
ENST00000422897.6:c.403C= ENSP00000407350.2:p.Arg135=
ENST00000457717.5:c.393+10C= ENSP00000400821.1:n.393+10C=
ENST00000506883.5:c.423+10C= ENSP00000426755.1:n.423+10C=
ENST00000511045.5:c.474+10C= ENSP00000427679.1:n.474+10C=
ENST00000619629.1:c.393+10C= ENSP00000482850.1:n.393+10C=
NM_000253.3:c.393+10C= NP_000244.2:n.393+10C=
NM_001300785.1:c.474+10C= NP_001287714.1:n.474+10C=
NM_000253.4:c.393+10C= NP_000244.2:n.393+10C=
NM_001300785.2:c.144+10C= NP_001287714.2:n.144+10C=
NM_001386140.1:c.393+10C= MANE Select NP_001373069.1:n.393+10C=