Canonical Allele Identifier: CA2762811655

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583549_99583550insACAG , CM000666.2:g.99583549_99583550insACAG	GRCh38
NC_000004.11:g.100504706_100504707insACAG , CM000666.1:g.100504706_100504707insACAG	GRCh37
NC_000004.10:g.100723729_100723730insACAG	NCBI36
NG_011469.1:g.24467_24468insACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.393+32_393+33insACAG MANE Select	ENSP00000265517.5:n.393+32_393+33insACAG
ENST00000457717.6:c.393+32_393+33insACAG	ENSP00000400821.1:n.393+32_393+33insACAG
ENST00000511045.6:c.144+32_144+33insACAG	ENSP00000427679.2:n.144+32_144+33insACAG
ENST00000265517.9:c.393+32_393+33insACAG	ENSP00000265517.5:n.393+32_393+33insACAG
ENST00000422897.6:c.425_426insACAG	ENSP00000407350.2:p.Pro143GlnfsTer17
ENST00000457717.5:c.393+32_393+33insACAG	ENSP00000400821.1:n.393+32_393+33insACAG
ENST00000506883.5:c.423+32_423+33insACAG	ENSP00000426755.1:n.423+32_423+33insACAG
ENST00000511045.5:c.474+32_474+33insACAG	ENSP00000427679.1:n.474+32_474+33insACAG
ENST00000619629.1:c.393+32_393+33insACAG	ENSP00000482850.1:n.393+32_393+33insACAG
NM_000253.3:c.393+32_393+33insACAG	NP_000244.2:n.393+32_393+33insACAG
NM_001300785.1:c.474+32_474+33insACAG	NP_001287714.1:n.474+32_474+33insACAG
NM_000253.4:c.393+32_393+33insACAG	NP_000244.2:n.393+32_393+33insACAG
NM_001300785.2:c.144+32_144+33insACAG	NP_001287714.2:n.144+32_144+33insACAG
NM_001386140.1:c.393+32_393+33insACAG MANE Select	NP_001373069.1:n.393+32_393+33insACAG