Canonical Allele Identifier: CA339973510
Gene: MPL HGNC NCBI

Linked Data

COSMIC: COSM909748

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338618G>T , CM000663.2:g.43338618G>T GRCh38
NC_000001.10:g.43804289G>T , CM000663.1:g.43804289G>T GRCh37
NC_000001.9:g.43576876G>T NCBI36
NG_007525.1:g.5815G>T , LRG_510:g.5815G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.289G>T MANE Select ENSP00000361548.3:p.Asp97Tyr
ENST00000413998.7:c.268G>T ENSP00000414004.3:p.Asp90Tyr
ENST00000638732.1:n.289G>T
ENST00000372470.7:c.289G>T ENSP00000361548.3:p.Asp97Tyr
ENST00000413998.6:c.289G>T ENSP00000414004.2:p.Asp97Tyr
ENST00000612993.1:c.289G>T ENSP00000480273.1:p.Asp97Tyr
NM_005373.2:c.289G>T , LRG_510t1:c.289G>T NP_005364.1:p.Asp97Tyr
XM_011541478.1:c.268G>T XP_011539780.1:p.Asp90Tyr
XM_017001320.1:c.460G>T XP_016856809.1:p.Asp154Tyr
NM_005373.3:c.289G>T MANE Select NP_005364.1:p.Asp97Tyr