Canonical Allele Identifier: CA2841605009
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349373del , CM000663.2:g.43349373del GRCh38
NC_000001.10:g.43815044del , CM000663.1:g.43815044del GRCh37
NC_000001.9:g.43587631del NCBI36
NG_007525.1:g.16570del , LRG_510:g.16570del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1565+14del MANE Select ENSP00000361548.3:n.1565+14del
ENST00000413998.7:c.1544+14del ENSP00000414004.3:n.1544+14del
ENST00000638732.1:n.1579del
ENST00000643351.1:c.97+14del
ENST00000372470.7:c.1565+14del ENSP00000361548.3:n.1565+14del
ENST00000413998.6:c.1579del ENSP00000414004.2:p.Gln527ArgfsTer15
ENST00000612993.1:c.1579del ENSP00000480273.1:p.Gln527ArgfsTer23
NM_005373.2:c.1565+14del , LRG_510t1:c.1565+14del NP_005364.1:n.1565+14del
XM_011541478.1:c.1544+14del XP_011539780.1:n.1544+14del
XM_017001320.1:c.1736+14del XP_016856809.1:n.1736+14del
NM_005373.3:c.1565+14del MANE Select NP_005364.1:n.1565+14del