Canonical Allele Identifier: CA1165576141
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338819T= , CM000663.2:g.43338819T= GRCh38
NC_000001.10:g.43804490T= , CM000663.1:g.43804490T= GRCh37
NC_000001.9:g.43577077T= NCBI36
NG_007525.1:g.6016T= , LRG_510:g.6016T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.391+99T= MANE Select ENSP00000361548.3:n.391+99T=
ENST00000413998.7:c.370+99T= ENSP00000414004.3:n.370+99T=
ENST00000638732.1:n.391+99T=
ENST00000372470.7:c.391+99T= ENSP00000361548.3:n.391+99T=
ENST00000413998.6:c.391+99T= ENSP00000414004.2:n.391+99T=
ENST00000612993.1:c.391+99T= ENSP00000480273.1:n.391+99T=
NM_005373.2:c.391+99T= , LRG_510t1:c.391+99T= NP_005364.1:n.391+99T=
XM_011541478.1:c.370+99T= XP_011539780.1:n.370+99T=
XM_017001320.1:c.562+99T= XP_016856809.1:n.562+99T=
NM_005373.3:c.391+99T= MANE Select NP_005364.1:n.391+99T=