Canonical Allele Identifier: CA2695806195

Gene: MPL

Linked Data

• dbSNP Id: rs2153916475

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338617_43338618insCTGCCTGGGATAGGTGG , CM000663.2:g.43338617_43338618insCTGCCTGGGATAGGTGG	GRCh38
NC_000001.10:g.43804288_43804289insCTGCCTGGGATAGGTGG , CM000663.1:g.43804288_43804289insCTGCCTGGGATAGGTGG	GRCh37
NC_000001.9:g.43576875_43576876insCTGCCTGGGATAGGTGG	NCBI36
NG_007525.1:g.5814_5815insCTGCCTGGGATAGGTGG , LRG_510:g.5814_5815insCTGCCTGGGATAGGTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000372470.9:c.288_289insCTGCCTGGGATAGGTGG MANE Select	ENSP00000361548.3:p.Asp97LeufsTer21
ENST00000413998.7:c.267_268insCTGCCTGGGATAGGTGG	ENSP00000414004.3:p.Asp90LeufsTer21
ENST00000638732.1:n.288_289insCTGCCTGGGATAGGTGG
ENST00000372470.7:c.288_289insCTGCCTGGGATAGGTGG	ENSP00000361548.3:p.Asp97LeufsTer21
ENST00000413998.6:c.288_289insCTGCCTGGGATAGGTGG	ENSP00000414004.2:p.Asp97LeufsTer21
ENST00000612993.1:c.288_289insCTGCCTGGGATAGGTGG	ENSP00000480273.1:p.Asp97LeufsTer21
NM_005373.2:c.288_289insCTGCCTGGGATAGGTGG , LRG_510t1:c.288_289insCTGCCTGGGATAGGTGG	NP_005364.1:p.Asp97LeufsTer21
XM_011541478.1:c.267_268insCTGCCTGGGATAGGTGG	XP_011539780.1:p.Asp90LeufsTer21
XM_017001320.1:c.459_460insCTGCCTGGGATAGGTGG	XP_016856809.1:p.Asp154LeufsTer21
NM_005373.3:c.288_289insCTGCCTGGGATAGGTGG MANE Select	NP_005364.1:p.Asp97LeufsTer21