Canonical Allele Identifier: CA2645226577
Gene: MPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349320del , CM000663.2:g.43349320del GRCh38
NC_000001.10:g.43814991del , CM000663.1:g.43814991del GRCh37
NC_000001.9:g.43587578del NCBI36
NG_007525.1:g.16517del , LRG_510:g.16517del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1526del MANE Select ENSP00000361548.3:p.Gly509AlafsTer5
ENST00000413998.7:c.1505del ENSP00000414004.3:p.Gly502AlafsTer5
ENST00000638732.1:n.1526del
ENST00000643351.1:c.58del
ENST00000372470.7:c.1526del ENSP00000361548.3:p.Gly509AlafsTer5
ENST00000413998.6:c.1526del ENSP00000414004.2:p.Gly509AlafsTer5
ENST00000612993.1:c.1526del ENSP00000480273.1:p.Gly509AlafsTer5
NM_005373.2:c.1526del , LRG_510t1:c.1526del NP_005364.1:p.Gly509AlafsTer5
XM_011541478.1:c.1505del XP_011539780.1:p.Gly502AlafsTer5
XM_017001320.1:c.1697del XP_016856809.1:p.Gly566AlafsTer5
NM_005373.3:c.1526del MANE Select NP_005364.1:p.Gly509AlafsTer5