Canonical Allele Identifier: CA2645221727
Gene: MPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337965del , CM000663.2:g.43337965del GRCh38
NC_000001.10:g.43803636del , CM000663.1:g.43803636del GRCh37
NC_000001.9:g.43576223del NCBI36
NG_007525.1:g.5162del , LRG_510:g.5162del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.79+38del MANE Select ENSP00000361548.3:n.79+38del
ENST00000413998.7:c.79+38del ENSP00000414004.3:n.79+38del
ENST00000638732.1:n.79+38del
ENST00000372470.7:c.79+38del ENSP00000361548.3:n.79+38del
ENST00000413998.6:c.79+38del ENSP00000414004.2:n.79+38del
ENST00000612993.1:c.79+38del ENSP00000480273.1:n.79+38del
NM_005373.2:c.79+38del , LRG_510t1:c.79+38del NP_005364.1:n.79+38del
XM_011541478.1:c.79+38del XP_011539780.1:n.79+38del
XM_017001320.1:c.117del XP_016856809.1:p.Lys40ArgfsTer7
NM_005373.3:c.79+38del MANE Select NP_005364.1:n.79+38del