Canonical Allele Identifier: CA1165575781
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337837G= , CM000663.2:g.43337837G= GRCh38
NC_000001.10:g.43803508G= , CM000663.1:g.43803508G= GRCh37
NC_000001.9:g.43576095G= NCBI36
NG_007525.1:g.5034G= , LRG_510:g.5034G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.-12G= MANE Select ENSP00000361548.3:n.-12G=
ENST00000372470.7:c.-12G= ENSP00000361548.3:n.-12G=
NM_005373.2:c.-12G= , LRG_510t1:c.-12G= NP_005364.1:n.-12G=
XM_011541478.1:c.-12G= XP_011539780.1:n.-12G=
XM_017001320.1:c.-12G= XP_016856809.1:n.-12G=
NM_005373.3:c.-12G= MANE Select NP_005364.1:n.-12G=