Canonical Allele Identifier: CA2695810601
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs2153916088

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337857_43337866del , CM000663.2:g.43337857_43337866del GRCh38
NC_000001.10:g.43803528_43803537del , CM000663.1:g.43803528_43803537del GRCh37
NC_000001.9:g.43576115_43576124del NCBI36
NG_007525.1:g.5054_5063del , LRG_510:g.5054_5063del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.9_18del MANE Select ENSP00000361548.3:p.Trp4SerfsTer?
ENST00000413998.7:c.9_18del ENSP00000414004.3:p.Trp4SerfsTer25
ENST00000638732.1:n.9_18del
ENST00000372470.7:c.9_18del ENSP00000361548.3:p.Trp4SerfsTer?
ENST00000413998.6:c.9_18del ENSP00000414004.2:p.Trp4SerfsTer?
ENST00000612993.1:c.9_18del ENSP00000480273.1:p.Trp4SerfsTer?
NM_005373.2:c.9_18del , LRG_510t1:c.9_18del NP_005364.1:p.Trp4SerfsTer?
XM_011541478.1:c.9_18del XP_011539780.1:p.Trp4SerfsTer25
XM_017001320.1:c.9_18del XP_016856809.1:p.Trp4SerfsTer?
NM_005373.3:c.9_18del MANE Select NP_005364.1:p.Trp4SerfsTer?