Canonical Allele Identifier: CA1165576080
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338636_43338637delinsCT , CM000663.2:g.43338636_43338637delinsCT GRCh38
NC_000001.10:g.43804307_43804308delinsCT , CM000663.1:g.43804307_43804308delinsCT GRCh37
NC_000001.9:g.43576894_43576895delinsCT NCBI36
NG_007525.1:g.5833_5834delinsCT , LRG_510:g.5833_5834delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.307_308delinsCT MANE Select ENSP00000361548.3:p.Leu103=
ENST00000413998.7:c.286_287delinsCT ENSP00000414004.3:p.Leu96=
ENST00000638732.1:n.307_308delinsCT
ENST00000372470.7:c.307_308delinsCT ENSP00000361548.3:p.Leu103=
ENST00000413998.6:c.307_308delinsCT ENSP00000414004.2:p.Leu103=
ENST00000612993.1:c.307_308delinsCT ENSP00000480273.1:p.Leu103=
NM_005373.2:c.307_308delinsCT , LRG_510t1:c.307_308delinsCT NP_005364.1:p.Leu103=
XM_011541478.1:c.286_287delinsCT XP_011539780.1:p.Leu96=
XM_017001320.1:c.478_479delinsCT XP_016856809.1:p.Leu160=
NM_005373.3:c.307_308delinsCT MANE Select NP_005364.1:p.Leu103=