Canonical Allele Identifier: CA916162771
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1553127595

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338497del , CM000663.2:g.43338497del GRCh38
NC_000001.10:g.43804168del , CM000663.1:g.43804168del GRCh37
NC_000001.9:g.43576755del NCBI36
NG_007525.1:g.5694del , LRG_510:g.5694del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.213-45del MANE Select ENSP00000361548.3:n.213-45del
ENST00000413998.7:c.192-45del ENSP00000414004.3:n.192-45del
ENST00000638732.1:n.213-45del
ENST00000372470.7:c.213-45del ENSP00000361548.3:n.213-45del
ENST00000413998.6:c.213-45del ENSP00000414004.2:n.213-45del
ENST00000612993.1:c.213-45del ENSP00000480273.1:n.213-45del
NM_005373.2:c.213-45del , LRG_510t1:c.213-45del NP_005364.1:n.213-45del
XM_011541478.1:c.192-45del XP_011539780.1:n.192-45del
XM_017001320.1:c.384-45del XP_016856809.1:n.384-45del
NM_005373.3:c.213-45del MANE Select NP_005364.1:n.213-45del