Canonical Allele Identifier: CA1480066929

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583672_99583673delinsTC , CM000666.2:g.99583672_99583673delinsTC	GRCh38
NC_000004.11:g.100504829_100504830delinsTC , CM000666.1:g.100504829_100504830delinsTC	GRCh37
NC_000004.10:g.100723852_100723853delinsTC	NCBI36
NG_011469.1:g.24590_24591delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.393+155_393+156delinsTC MANE Select	ENSP00000265517.5:n.393+155_393+156delinsTC
ENST00000457717.6:c.393+155_393+156delinsTC	ENSP00000400821.1:n.393+155_393+156delinsTC
ENST00000511045.6:c.144+155_144+156delinsTC	ENSP00000427679.2:n.144+155_144+156delinsTC
ENST00000265517.9:c.393+155_393+156delinsTC	ENSP00000265517.5:n.393+155_393+156delinsTC
ENST00000422897.6:c.*92_*93delinsTC	ENSP00000407350.2:n.*92_*93delinsTC
ENST00000457717.5:c.393+155_393+156delinsTC	ENSP00000400821.1:n.393+155_393+156delinsTC
ENST00000506883.5:c.423+155_423+156delinsTC	ENSP00000426755.1:n.423+155_423+156delinsTC
ENST00000511045.5:c.474+155_474+156delinsTC	ENSP00000427679.1:n.474+155_474+156delinsTC
ENST00000619629.1:c.393+155_393+156delinsTC	ENSP00000482850.1:n.393+155_393+156delinsTC
NM_000253.3:c.393+155_393+156delinsTC	NP_000244.2:n.393+155_393+156delinsTC
NM_001300785.1:c.474+155_474+156delinsTC	NP_001287714.1:n.474+155_474+156delinsTC
NM_000253.4:c.393+155_393+156delinsTC	NP_000244.2:n.393+155_393+156delinsTC
NM_001300785.2:c.144+155_144+156delinsTC	NP_001287714.2:n.144+155_144+156delinsTC
NM_001386140.1:c.393+155_393+156delinsTC MANE Select	NP_001373069.1:n.393+155_393+156delinsTC