Canonical Allele Identifier: CA1148224238
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338705_43338707delinsTTT , CM000663.2:g.43338705_43338707delinsTTT GRCh38
NC_000001.10:g.43804376_43804378delinsTTT , CM000663.1:g.43804376_43804378delinsTTT GRCh37
NC_000001.9:g.43576963_43576965delinsTTT NCBI36
NG_007525.1:g.5902_5904delinsTTT , LRG_510:g.5902_5904delinsTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.376_378delinsTTT MANE Select ENSP00000361548.3:p.Phe126=
ENST00000413998.7:c.355_357delinsTTT ENSP00000414004.3:p.Phe119=
ENST00000638732.1:n.376_378delinsTTT
ENST00000372470.7:c.376_378delinsTTT ENSP00000361548.3:p.Phe126=
ENST00000413998.6:c.376_378delinsTTT ENSP00000414004.2:p.Phe126=
ENST00000612993.1:c.376_378delinsTTT ENSP00000480273.1:p.Phe126=
NM_005373.2:c.376_378delinsTTT , LRG_510t1:c.376_378delinsTTT NP_005364.1:p.Phe126=
XM_011541478.1:c.355_357delinsTTT XP_011539780.1:p.Phe119=
XM_017001320.1:c.547_549delinsTTT XP_016856809.1:p.Phe183=
NM_005373.3:c.376_378delinsTTT MANE Select NP_005364.1:p.Phe126=