Canonical Allele Identifier: CA1480066409
Gene: MTTP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99583245_99583246delinsTG , CM000666.2:g.99583245_99583246delinsTG GRCh38
NC_000004.11:g.100504402_100504403delinsTG , CM000666.1:g.100504402_100504403delinsTG GRCh37
NC_000004.10:g.100723425_100723426delinsTG NCBI36
NG_011469.1:g.24163_24164delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265517.10:c.250-129_250-128delinsTG MANE Select ENSP00000265517.5:n.250-129_250-128delinsTG
ENST00000457717.6:c.250-129_250-128delinsTG ENSP00000400821.1:n.250-129_250-128delinsTG
ENST00000505094.6:c.1-129_1-128delinsTG ENSP00000422782.2:n.1-129_1-128delinsTG
ENST00000511045.6:c.1-129_1-128delinsTG ENSP00000427679.2:n.1-129_1-128delinsTG
ENST00000265517.9:c.250-129_250-128delinsTG ENSP00000265517.5:n.250-129_250-128delinsTG
ENST00000422897.6:c.250-129_250-128delinsTG ENSP00000407350.2:n.250-129_250-128delinsTG
ENST00000457717.5:c.250-129_250-128delinsTG ENSP00000400821.1:n.250-129_250-128delinsTG
ENST00000505094.5:c.*340-129_*340-128delinsTG ENSP00000422782.1:n.*340-129_*340-128delinsTG
ENST00000506883.5:c.280-129_280-128delinsTG ENSP00000426755.1:n.280-129_280-128delinsTG
ENST00000511045.5:c.331-129_331-128delinsTG ENSP00000427679.1:n.331-129_331-128delinsTG
ENST00000513404.5:c.*313-129_*313-128delinsTG ENSP00000424972.1:n.*313-129_*313-128delinsTG
ENST00000515141.5:c.*313-129_*313-128delinsTG ENSP00000425642.1:n.*313-129_*313-128delinsTG
ENST00000619629.1:c.250-129_250-128delinsTG ENSP00000482850.1:n.250-129_250-128delinsTG
NM_000253.3:c.250-129_250-128delinsTG NP_000244.2:n.250-129_250-128delinsTG
NM_001300785.1:c.331-129_331-128delinsTG NP_001287714.1:n.331-129_331-128delinsTG
NM_000253.4:c.250-129_250-128delinsTG NP_000244.2:n.250-129_250-128delinsTG
NM_001300785.2:c.1-129_1-128delinsTG NP_001287714.2:n.1-129_1-128delinsTG
NM_001386140.1:c.250-129_250-128delinsTG MANE Select NP_001373069.1:n.250-129_250-128delinsTG