Canonical Allele Identifier: CA2762810706

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583581_99583582insG , CM000666.2:g.99583581_99583582insG	GRCh38
NC_000004.11:g.100504738_100504739insG , CM000666.1:g.100504738_100504739insG	GRCh37
NC_000004.10:g.100723761_100723762insG	NCBI36
NG_011469.1:g.24499_24500insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.393+64_393+65insG MANE Select	ENSP00000265517.5:n.393+64_393+65insG
ENST00000457717.6:c.393+64_393+65insG	ENSP00000400821.1:n.393+64_393+65insG
ENST00000511045.6:c.144+64_144+65insG	ENSP00000427679.2:n.144+64_144+65insG
ENST00000265517.9:c.393+64_393+65insG	ENSP00000265517.5:n.393+64_393+65insG
ENST00000422897.6:c.*1_*2insG	ENSP00000407350.2:n.*1_*2insG
ENST00000457717.5:c.393+64_393+65insG	ENSP00000400821.1:n.393+64_393+65insG
ENST00000506883.5:c.423+64_423+65insG	ENSP00000426755.1:n.423+64_423+65insG
ENST00000511045.5:c.474+64_474+65insG	ENSP00000427679.1:n.474+64_474+65insG
ENST00000619629.1:c.393+64_393+65insG	ENSP00000482850.1:n.393+64_393+65insG
NM_000253.3:c.393+64_393+65insG	NP_000244.2:n.393+64_393+65insG
NM_001300785.1:c.474+64_474+65insG	NP_001287714.1:n.474+64_474+65insG
NM_000253.4:c.393+64_393+65insG	NP_000244.2:n.393+64_393+65insG
NM_001300785.2:c.144+64_144+65insG	NP_001287714.2:n.144+64_144+65insG
NM_001386140.1:c.393+64_393+65insG MANE Select	NP_001373069.1:n.393+64_393+65insG