Canonical Allele Identifier: CA2645222041
Gene: MPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338387del , CM000663.2:g.43338387del GRCh38
NC_000001.10:g.43804058del , CM000663.1:g.43804058del GRCh37
NC_000001.9:g.43576645del NCBI36
NG_007525.1:g.5584del , LRG_510:g.5584del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.213-155del MANE Select ENSP00000361548.3:n.213-155del
ENST00000413998.7:c.192-155del ENSP00000414004.3:n.192-155del
ENST00000638732.1:n.213-155del
ENST00000372470.7:c.213-155del ENSP00000361548.3:n.213-155del
ENST00000413998.6:c.213-155del ENSP00000414004.2:n.213-155del
ENST00000612993.1:c.213-155del ENSP00000480273.1:n.213-155del
NM_005373.2:c.213-155del , LRG_510t1:c.213-155del NP_005364.1:n.213-155del
XM_011541478.1:c.192-155del XP_011539780.1:n.192-155del
XM_017001320.1:c.384-155del XP_016856809.1:n.384-155del
NM_005373.3:c.213-155del MANE Select NP_005364.1:n.213-155del