Canonical Allele Identifier: CA1165576101
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338702_43338703delinsCT , CM000663.2:g.43338702_43338703delinsCT GRCh38
NC_000001.10:g.43804373_43804374delinsCT , CM000663.1:g.43804373_43804374delinsCT GRCh37
NC_000001.9:g.43576960_43576961delinsCT NCBI36
NG_007525.1:g.5899_5900delinsCT , LRG_510:g.5899_5900delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.373_374delinsCT MANE Select ENSP00000361548.3:p.Leu125=
ENST00000413998.7:c.352_353delinsCT ENSP00000414004.3:p.Leu118=
ENST00000638732.1:n.373_374delinsCT
ENST00000372470.7:c.373_374delinsCT ENSP00000361548.3:p.Leu125=
ENST00000413998.6:c.373_374delinsCT ENSP00000414004.2:p.Leu125=
ENST00000612993.1:c.373_374delinsCT ENSP00000480273.1:p.Leu125=
NM_005373.2:c.373_374delinsCT , LRG_510t1:c.373_374delinsCT NP_005364.1:p.Leu125=
XM_011541478.1:c.352_353delinsCT XP_011539780.1:p.Leu118=
XM_017001320.1:c.544_545delinsCT XP_016856809.1:p.Leu182=
NM_005373.3:c.373_374delinsCT MANE Select NP_005364.1:p.Leu125=