Canonical Allele Identifier: CA1480079140
Gene: MTTP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99600553_99600554delinsCT , CM000666.2:g.99600553_99600554delinsCT GRCh38
NC_000004.11:g.100521710_100521711delinsCT , CM000666.1:g.100521710_100521711delinsCT GRCh37
NC_000004.10:g.100740733_100740734delinsCT NCBI36
NG_011469.1:g.41471_41472delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000265517.10:c.1068-12_1068-11delinsCT MANE Select ENSP00000265517.5:n.1068-12_1068-11delins...
ENST00000457717.6:c.1068-12_1068-11delinsCT ENSP00000400821.1:n.1068-12_1068-11delins...
ENST00000511045.6:c.819-12_819-11delinsCT ENSP00000427679.2:n.819-12_819-11delinsCT...
ENST00000265517.9:c.1068-12_1068-11delinsCT ENSP00000265517.5:n.1068-12_1068-11delins...
ENST00000457717.5:c.1068-12_1068-11delinsCT ENSP00000400821.1:n.1068-12_1068-11delins...
ENST00000511045.5:c.1149-12_1149-11delinsCT ENSP00000427679.1:n.1149-12_1149-11delins...
ENST00000619629.1:c.1068-12_1068-11delinsCT ENSP00000482850.1:n.1068-12_1068-11delins...
NM_000253.3:c.1068-12_1068-11delinsCT NP_000244.2:n.1068-12_1068-11delinsCT
NM_001300785.1:c.1149-12_1149-11delinsCT NP_001287714.1:n.1149-12_1149-11delinsCT
NM_000253.4:c.1068-12_1068-11delinsCT NP_000244.2:n.1068-12_1068-11delinsCT
NM_001300785.2:c.819-12_819-11delinsCT NP_001287714.2:n.819-12_819-11delinsCT
NM_001386140.1:c.1068-12_1068-11delinsCT MANE Select NP_001373069.1:n.1068-12_1068-11delinsCT