Canonical Allele Identifier: CA2574340713
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs2153916175

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338039del , CM000663.2:g.43338039del GRCh38
NC_000001.10:g.43803710del , CM000663.1:g.43803710del GRCh37
NC_000001.9:g.43576297del NCBI36
NG_007525.1:g.5236del , LRG_510:g.5236del

Transcript Alleles

HGVS Amino-acid change
ENST00000372470.9:c.80-60del MANE Select ENSP00000361548.3:n.80-60del
ENST00000413998.7:c.80-81del ENSP00000414004.3:n.80-81del
ENST00000638732.1:n.80-60del
ENST00000372470.7:c.80-60del ENSP00000361548.3:n.80-60del
ENST00000413998.6:c.80-60del ENSP00000414004.2:n.80-60del
ENST00000612993.1:c.80-60del ENSP00000480273.1:n.80-60del
NM_005373.2:c.80-60del , LRG_510t1:c.80-60del NP_005364.1:n.80-60del
XM_011541478.1:c.80-81del XP_011539780.1:n.80-81del
XM_017001320.1:c.191del XP_016856809.1:p.Leu64ProfsTer5
NM_005373.3:c.80-60del MANE Select NP_005364.1:n.80-60del