Canonical Allele Identifier: CA1001097301
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1647005932

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338049_43338050dup , CM000663.2:g.43338049_43338050dup GRCh38
NC_000001.10:g.43803720_43803721dup , CM000663.1:g.43803720_43803721dup GRCh37
NC_000001.9:g.43576307_43576308dup NCBI36
NG_007525.1:g.5246_5247dup , LRG_510:g.5246_5247dup

Transcript Alleles

HGVS Amino-acid change
ENST00000372470.9:c.80-50_80-49dup MANE Select ENSP00000361548.3:n.80-50_80-49dup
ENST00000413998.7:c.80-71_80-70dup ENSP00000414004.3:n.80-71_80-70dup
ENST00000638732.1:n.80-50_80-49dup
ENST00000372470.7:c.80-50_80-49dup ENSP00000361548.3:n.80-50_80-49dup
ENST00000413998.6:c.80-50_80-49dup ENSP00000414004.2:n.80-50_80-49dup
ENST00000612993.1:c.80-50_80-49dup ENSP00000480273.1:n.80-50_80-49dup
NM_005373.2:c.80-50_80-49dup , LRG_510t1:c.80-50_80-49dup NP_005364.1:n.80-50_80-49dup
XM_011541478.1:c.80-71_80-70dup XP_011539780.1:n.80-71_80-70dup
XM_017001320.1:c.201_202dup XP_016856809.1:p.Ile68ThrfsTer2
NM_005373.3:c.80-50_80-49dup MANE Select NP_005364.1:n.80-50_80-49dup