Canonical Allele Identifier: CA1480066247
Gene: MTTP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99583014_99583015delinsAG , CM000666.2:g.99583014_99583015delinsAG GRCh38
NC_000004.11:g.100504171_100504172delinsAG , CM000666.1:g.100504171_100504172delinsAG GRCh37
NC_000004.10:g.100723194_100723195delinsAG NCBI36
NG_011469.1:g.23932_23933delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265517.10:c.250-360_250-359delinsAG MANE Select ENSP00000265517.5:n.250-360_250-359delinsAG
ENST00000457717.6:c.250-360_250-359delinsAG ENSP00000400821.1:n.250-360_250-359delinsAG
ENST00000505094.6:c.1-360_1-359delinsAG ENSP00000422782.2:n.1-360_1-359delinsAG
ENST00000511045.6:c.1-360_1-359delinsAG ENSP00000427679.2:n.1-360_1-359delinsAG
ENST00000265517.9:c.250-360_250-359delinsAG ENSP00000265517.5:n.250-360_250-359delinsAG
ENST00000422897.6:c.250-360_250-359delinsAG ENSP00000407350.2:n.250-360_250-359delinsAG
ENST00000457717.5:c.250-360_250-359delinsAG ENSP00000400821.1:n.250-360_250-359delinsAG
ENST00000505094.5:c.*340-360_*340-359delinsAG ENSP00000422782.1:n.*340-360_*340-359delinsAG
ENST00000506883.5:c.280-360_280-359delinsAG ENSP00000426755.1:n.280-360_280-359delinsAG
ENST00000511045.5:c.331-360_331-359delinsAG ENSP00000427679.1:n.331-360_331-359delinsAG
ENST00000513404.5:c.*313-360_*313-359delinsAG ENSP00000424972.1:n.*313-360_*313-359delinsAG
ENST00000515141.5:c.*313-360_*313-359delinsAG ENSP00000425642.1:n.*313-360_*313-359delinsAG
ENST00000619629.1:c.250-360_250-359delinsAG ENSP00000482850.1:n.250-360_250-359delinsAG
NM_000253.3:c.250-360_250-359delinsAG NP_000244.2:n.250-360_250-359delinsAG
NM_001300785.1:c.331-360_331-359delinsAG NP_001287714.1:n.331-360_331-359delinsAG
NM_000253.4:c.250-360_250-359delinsAG NP_000244.2:n.250-360_250-359delinsAG
NM_001300785.2:c.1-360_1-359delinsAG NP_001287714.2:n.1-360_1-359delinsAG
NM_001386140.1:c.250-360_250-359delinsAG MANE Select NP_001373069.1:n.250-360_250-359delinsAG