Canonical Allele Identifier: CA1165576077
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338628A= , CM000663.2:g.43338628A= GRCh38
NC_000001.10:g.43804299A= , CM000663.1:g.43804299A= GRCh37
NC_000001.9:g.43576886A= NCBI36
NG_007525.1:g.5825A= , LRG_510:g.5825A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.299A= MANE Select ENSP00000361548.3:p.Glu100=
ENST00000413998.7:c.278A= ENSP00000414004.3:p.Glu93=
ENST00000638732.1:n.299A=
ENST00000372470.7:c.299A= ENSP00000361548.3:p.Glu100=
ENST00000413998.6:c.299A= ENSP00000414004.2:p.Glu100=
ENST00000612993.1:c.299A= ENSP00000480273.1:p.Glu100=
NM_005373.2:c.299A= , LRG_510t1:c.299A= NP_005364.1:p.Glu100=
XM_011541478.1:c.278A= XP_011539780.1:p.Glu93=
XM_017001320.1:c.470A= XP_016856809.1:p.Glu157=
NM_005373.3:c.299A= MANE Select NP_005364.1:p.Glu100=