Canonical Allele Identifier: CA1165580065
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349352C= , CM000663.2:g.43349352C= GRCh38
NC_000001.10:g.43815023C= , CM000663.1:g.43815023C= GRCh37
NC_000001.9:g.43587610C= NCBI36
NG_007525.1:g.16549C= , LRG_510:g.16549C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1558C= MANE Select ENSP00000361548.3:p.His520=
ENST00000413998.7:c.1537C= ENSP00000414004.3:p.His513=
ENST00000638732.1:n.1558C=
ENST00000643351.1:c.90C=
ENST00000372470.7:c.1558C= ENSP00000361548.3:p.His520=
ENST00000413998.6:c.1558C= ENSP00000414004.2:p.His520=
ENST00000612993.1:c.1558C= ENSP00000480273.1:p.His520=
NM_005373.2:c.1558C= , LRG_510t1:c.1558C= NP_005364.1:p.His520=
XM_011541478.1:c.1537C= XP_011539780.1:p.His513=
XM_017001320.1:c.1729C= XP_016856809.1:p.His577=
NM_005373.3:c.1558C= MANE Select NP_005364.1:p.His520=