Canonical Allele Identifier: CA1165576026
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338488_43338489delinsTC , CM000663.2:g.43338488_43338489delinsTC GRCh38
NC_000001.10:g.43804159_43804160delinsTC , CM000663.1:g.43804159_43804160delinsTC GRCh37
NC_000001.9:g.43576746_43576747delinsTC NCBI36
NG_007525.1:g.5685_5686delinsTC , LRG_510:g.5685_5686delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.213-54_213-53delinsTC MANE Select ENSP00000361548.3:n.213-54_213-53delinsTC
ENST00000413998.7:c.192-54_192-53delinsTC ENSP00000414004.3:n.192-54_192-53delinsTC
ENST00000638732.1:n.213-54_213-53delinsTC
ENST00000372470.7:c.213-54_213-53delinsTC ENSP00000361548.3:n.213-54_213-53delinsTC
ENST00000413998.6:c.213-54_213-53delinsTC ENSP00000414004.2:n.213-54_213-53delinsTC
ENST00000612993.1:c.213-54_213-53delinsTC ENSP00000480273.1:n.213-54_213-53delinsTC
NM_005373.2:c.213-54_213-53delinsTC , LRG_510t1:c.213-54_213-53delinsTC NP_005364.1:n.213-54_213-53delinsTC
XM_011541478.1:c.192-54_192-53delinsTC XP_011539780.1:n.192-54_192-53delinsTC
XM_017001320.1:c.384-54_384-53delinsTC XP_016856809.1:n.384-54_384-53delinsTC
NM_005373.3:c.213-54_213-53delinsTC MANE Select NP_005364.1:n.213-54_213-53delinsTC