Canonical Allele Identifier: CA2841605006
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349302del , CM000663.2:g.43349302del GRCh38
NC_000001.10:g.43814973del , CM000663.1:g.43814973del GRCh37
NC_000001.9:g.43587560del NCBI36
NG_007525.1:g.16499del , LRG_510:g.16499del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1508del MANE Select ENSP00000361548.3:p.Gly503AlafsTer11
ENST00000413998.7:c.1487del ENSP00000414004.3:p.Gly496AlafsTer11
ENST00000638732.1:n.1508del
ENST00000643351.1:c.40del
ENST00000372470.7:c.1508del ENSP00000361548.3:p.Gly503AlafsTer11
ENST00000413998.6:c.1508del ENSP00000414004.2:p.Gly503AlafsTer11
ENST00000612993.1:c.1508del ENSP00000480273.1:p.Gly503AlafsTer11
NM_005373.2:c.1508del , LRG_510t1:c.1508del NP_005364.1:p.Gly503AlafsTer11
XM_011541478.1:c.1487del XP_011539780.1:p.Gly496AlafsTer11
XM_017001320.1:c.1679del XP_016856809.1:p.Gly560AlafsTer11
NM_005373.3:c.1508del MANE Select NP_005364.1:p.Gly503AlafsTer11