Canonical Allele Identifier: CA2762811656

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583554_99583555insAGG , CM000666.2:g.99583554_99583555insAGG	GRCh38
NC_000004.11:g.100504711_100504712insAGG , CM000666.1:g.100504711_100504712insAGG	GRCh37
NC_000004.10:g.100723734_100723735insAGG	NCBI36
NG_011469.1:g.24472_24473insAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.393+37_393+38insAGG MANE Select	ENSP00000265517.5:n.393+37_393+38insAGG
ENST00000457717.6:c.393+37_393+38insAGG	ENSP00000400821.1:n.393+37_393+38insAGG
ENST00000511045.6:c.144+37_144+38insAGG	ENSP00000427679.2:n.144+37_144+38insAGG
ENST00000265517.9:c.393+37_393+38insAGG	ENSP00000265517.5:n.393+37_393+38insAGG
ENST00000422897.6:c.430_431insAGG	ENSP00000407350.2:p.Thr144delinsLysAla
ENST00000457717.5:c.393+37_393+38insAGG	ENSP00000400821.1:n.393+37_393+38insAGG
ENST00000506883.5:c.423+37_423+38insAGG	ENSP00000426755.1:n.423+37_423+38insAGG
ENST00000511045.5:c.474+37_474+38insAGG	ENSP00000427679.1:n.474+37_474+38insAGG
ENST00000619629.1:c.393+37_393+38insAGG	ENSP00000482850.1:n.393+37_393+38insAGG
NM_000253.3:c.393+37_393+38insAGG	NP_000244.2:n.393+37_393+38insAGG
NM_001300785.1:c.474+37_474+38insAGG	NP_001287714.1:n.474+37_474+38insAGG
NM_000253.4:c.393+37_393+38insAGG	NP_000244.2:n.393+37_393+38insAGG
NM_001300785.2:c.144+37_144+38insAGG	NP_001287714.2:n.144+37_144+38insAGG
NM_001386140.1:c.393+37_393+38insAGG MANE Select	NP_001373069.1:n.393+37_393+38insAGG