Canonical Allele Identifier: CA2762811652

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583546_99583547insA , CM000666.2:g.99583546_99583547insA	GRCh38
NC_000004.11:g.100504703_100504704insA , CM000666.1:g.100504703_100504704insA	GRCh37
NC_000004.10:g.100723726_100723727insA	NCBI36
NG_011469.1:g.24464_24465insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.393+29_393+30insA MANE Select	ENSP00000265517.5:n.393+29_393+30insA
ENST00000457717.6:c.393+29_393+30insA	ENSP00000400821.1:n.393+29_393+30insA
ENST00000511045.6:c.144+29_144+30insA	ENSP00000427679.2:n.144+29_144+30insA
ENST00000265517.9:c.393+29_393+30insA	ENSP00000265517.5:n.393+29_393+30insA
ENST00000422897.6:c.422_423insA	ENSP00000407350.2:p.Phe141LeufsTer18
ENST00000457717.5:c.393+29_393+30insA	ENSP00000400821.1:n.393+29_393+30insA
ENST00000506883.5:c.423+29_423+30insA	ENSP00000426755.1:n.423+29_423+30insA
ENST00000511045.5:c.474+29_474+30insA	ENSP00000427679.1:n.474+29_474+30insA
ENST00000619629.1:c.393+29_393+30insA	ENSP00000482850.1:n.393+29_393+30insA
NM_000253.3:c.393+29_393+30insA	NP_000244.2:n.393+29_393+30insA
NM_001300785.1:c.474+29_474+30insA	NP_001287714.1:n.474+29_474+30insA
NM_000253.4:c.393+29_393+30insA	NP_000244.2:n.393+29_393+30insA
NM_001300785.2:c.144+29_144+30insA	NP_001287714.2:n.144+29_144+30insA
NM_001386140.1:c.393+29_393+30insA MANE Select	NP_001373069.1:n.393+29_393+30insA