Canonical Allele Identifier: CA2762811664

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583568_99583569insACA , CM000666.2:g.99583568_99583569insACA	GRCh38
NC_000004.11:g.100504725_100504726insACA , CM000666.1:g.100504725_100504726insACA	GRCh37
NC_000004.10:g.100723748_100723749insACA	NCBI36
NG_011469.1:g.24486_24487insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.393+51_393+52insACA MANE Select	ENSP00000265517.5:n.393+51_393+52insACA
ENST00000457717.6:c.393+51_393+52insACA	ENSP00000400821.1:n.393+51_393+52insACA
ENST00000511045.6:c.144+51_144+52insACA	ENSP00000427679.2:n.144+51_144+52insACA
ENST00000265517.9:c.393+51_393+52insACA	ENSP00000265517.5:n.393+51_393+52insACA
ENST00000422897.6:c.444_445insACA	ENSP00000407350.2:p.Ser148_Ser149insThr
ENST00000457717.5:c.393+51_393+52insACA	ENSP00000400821.1:n.393+51_393+52insACA
ENST00000506883.5:c.423+51_423+52insACA	ENSP00000426755.1:n.423+51_423+52insACA
ENST00000511045.5:c.474+51_474+52insACA	ENSP00000427679.1:n.474+51_474+52insACA
ENST00000619629.1:c.393+51_393+52insACA	ENSP00000482850.1:n.393+51_393+52insACA
NM_000253.3:c.393+51_393+52insACA	NP_000244.2:n.393+51_393+52insACA
NM_001300785.1:c.474+51_474+52insACA	NP_001287714.1:n.474+51_474+52insACA
NM_000253.4:c.393+51_393+52insACA	NP_000244.2:n.393+51_393+52insACA
NM_001300785.2:c.144+51_144+52insACA	NP_001287714.2:n.144+51_144+52insACA
NM_001386140.1:c.393+51_393+52insACA MANE Select	NP_001373069.1:n.393+51_393+52insACA