Canonical Allele Identifier: CA1480066794

Gene: MTTP

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99583557_99583559delinsTCA , CM000666.2:g.99583557_99583559delinsTCA	GRCh38
NC_000004.11:g.100504714_100504716delinsTCA , CM000666.1:g.100504714_100504716delinsTCA	GRCh37
NC_000004.10:g.100723737_100723739delinsTCA	NCBI36
NG_011469.1:g.24475_24477delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265517.10:c.393+40_393+42delinsTCA MANE Select	ENSP00000265517.5:n.393+40_393+42delinsTCA
ENST00000457717.6:c.393+40_393+42delinsTCA	ENSP00000400821.1:n.393+40_393+42delinsTCA
ENST00000511045.6:c.144+40_144+42delinsTCA	ENSP00000427679.2:n.144+40_144+42delinsTCA
ENST00000265517.9:c.393+40_393+42delinsTCA	ENSP00000265517.5:n.393+40_393+42delinsTCA
ENST00000422897.6:c.433_435delinsTCA	ENSP00000407350.2:p.Ser145=
ENST00000457717.5:c.393+40_393+42delinsTCA	ENSP00000400821.1:n.393+40_393+42delinsTCA
ENST00000506883.5:c.423+40_423+42delinsTCA	ENSP00000426755.1:n.423+40_423+42delinsTCA
ENST00000511045.5:c.474+40_474+42delinsTCA	ENSP00000427679.1:n.474+40_474+42delinsTCA
ENST00000619629.1:c.393+40_393+42delinsTCA	ENSP00000482850.1:n.393+40_393+42delinsTCA
NM_000253.3:c.393+40_393+42delinsTCA	NP_000244.2:n.393+40_393+42delinsTCA
NM_001300785.1:c.474+40_474+42delinsTCA	NP_001287714.1:n.474+40_474+42delinsTCA
NM_000253.4:c.393+40_393+42delinsTCA	NP_000244.2:n.393+40_393+42delinsTCA
NM_001300785.2:c.144+40_144+42delinsTCA	NP_001287714.2:n.144+40_144+42delinsTCA
NM_001386140.1:c.393+40_393+42delinsTCA MANE Select	NP_001373069.1:n.393+40_393+42delinsTCA