Canonical Allele Identifier: CA1480086349
Gene: MTTP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99618658_99618661delinsCTGT , CM000666.2:g.99618658_99618661delinsCTGT GRCh38
NC_000004.11:g.100539815_100539818delinsCTGT , CM000666.1:g.100539815_100539818delinsCTGT GRCh37
NC_000004.10:g.100758838_100758841delinsCTGT NCBI36
NG_011469.1:g.59576_59579delinsCTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000265517.10:c.2218-316_2218-313delinsCTGT MANE Select ENSP00000265517.5:n.2218-316_2218-313deli...
ENST00000457717.6:c.2218-316_2218-313delinsCTGT ENSP00000400821.1:n.2218-316_2218-313deli...
ENST00000511045.6:c.1969-316_1969-313delinsCTGT ENSP00000427679.2:n.1969-316_1969-313deli...
ENST00000265517.9:c.2218-316_2218-313delinsCTGT ENSP00000265517.5:n.2218-316_2218-313deli...
ENST00000457717.5:c.2218-316_2218-313delinsCTGT ENSP00000400821.1:n.2218-316_2218-313deli...
ENST00000511045.5:c.2299-316_2299-313delinsCTGT ENSP00000427679.1:n.2299-316_2299-313deli...
ENST00000619629.1:c.*665-316_*665-313delinsCTGT ENSP00000482850.1:n.*665-316_*665-313deli...
NM_000253.3:c.2218-316_2218-313delinsCTGT NP_000244.2:n.2218-316_2218-313delinsCTGT...
NM_001300785.1:c.2299-316_2299-313delinsCTGT NP_001287714.1:n.2299-316_2299-313delinsC...
NM_000253.4:c.2218-316_2218-313delinsCTGT NP_000244.2:n.2218-316_2218-313delinsCTGT...
NM_001300785.2:c.1969-316_1969-313delinsCTGT NP_001287714.2:n.1969-316_1969-313delinsC...
NM_001386140.1:c.2218-316_2218-313delinsCTGT MANE Select NP_001373069.1:n.2218-316_2218-313delinsC...