Canonical Allele Identifier: CA1144044792
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43352788T= , CM000663.2:g.43352788T= GRCh38
NC_000001.10:g.43818459T= , CM000663.1:g.43818459T= GRCh37
NC_000001.9:g.43591046T= NCBI36
NG_007525.1:g.19985T= , LRG_510:g.19985T=

Transcript Alleles

HGVS Amino-acid change
ENST00000372470.9:c.*16T= MANE Select ENSP00000361548.3:n.*16T=
NM_005373.2:c.*16T= , LRG_510t1:c.*16T= NP_005364.1:n.*16T=
XM_011541478.1:c.*16T= XP_011539780.1:n.*16T=
XM_017001320.1:c.*16T= XP_016856809.1:n.*16T=
NM_005373.3:c.*16T= MANE Select NP_005364.1:n.*16T=