Canonical Allele Identifier: CA1165575821
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337973A= , CM000663.2:g.43337973A= GRCh38
NC_000001.10:g.43803644A= , CM000663.1:g.43803644A= GRCh37
NC_000001.9:g.43576231A= NCBI36
NG_007525.1:g.5170A= , LRG_510:g.5170A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.79+46A= MANE Select ENSP00000361548.3:n.79+46A=
ENST00000413998.7:c.79+46A= ENSP00000414004.3:n.79+46A=
ENST00000638732.1:n.79+46A=
ENST00000372470.7:c.79+46A= ENSP00000361548.3:n.79+46A=
ENST00000413998.6:c.79+46A= ENSP00000414004.2:n.79+46A=
ENST00000612993.1:c.79+46A= ENSP00000480273.1:n.79+46A=
NM_005373.2:c.79+46A= , LRG_510t1:c.79+46A= NP_005364.1:n.79+46A=
XM_011541478.1:c.79+46A= XP_011539780.1:n.79+46A=
XM_017001320.1:c.125A= XP_016856809.1:p.Glu42=
NM_005373.3:c.79+46A= MANE Select NP_005364.1:n.79+46A=