Canonical Allele Identifier: CA1165579727
Gene: MPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349167A= , CM000663.2:g.43349167A= GRCh38
NC_000001.10:g.43814838A= , CM000663.1:g.43814838A= GRCh37
NC_000001.9:g.43587425A= NCBI36
NG_007525.1:g.16364A= , LRG_510:g.16364A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1469-96A= MANE Select ENSP00000361548.3:n.1469-96A=
ENST00000413998.7:c.1448-96A= ENSP00000414004.3:n.1448-96A=
ENST00000638732.1:n.1469-96A=
ENST00000372470.7:c.1469-96A= ENSP00000361548.3:n.1469-96A=
ENST00000413998.6:c.1469-96A= ENSP00000414004.2:n.1469-96A=
ENST00000612993.1:c.1469-96A= ENSP00000480273.1:n.1469-96A=
NM_005373.2:c.1469-96A= , LRG_510t1:c.1469-96A= NP_005364.1:n.1469-96A=
XM_011541478.1:c.1448-96A= XP_011539780.1:n.1448-96A=
XM_017001320.1:c.1640-96A= XP_016856809.1:n.1640-96A=
NM_005373.3:c.1469-96A= MANE Select NP_005364.1:n.1469-96A=
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