Canonical Allele Identifier: CA1165576094
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338681C= , CM000663.2:g.43338681C= GRCh38
NC_000001.10:g.43804352C= , CM000663.1:g.43804352C= GRCh37
NC_000001.9:g.43576939C= NCBI36
NG_007525.1:g.5878C= , LRG_510:g.5878C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.352C= MANE Select ENSP00000361548.3:p.Gln118=
ENST00000413998.7:c.331C= ENSP00000414004.3:p.Gln111=
ENST00000638732.1:n.352C=
ENST00000372470.7:c.352C= ENSP00000361548.3:p.Gln118=
ENST00000413998.6:c.352C= ENSP00000414004.2:p.Gln118=
ENST00000612993.1:c.352C= ENSP00000480273.1:p.Gln118=
NM_005373.2:c.352C= , LRG_510t1:c.352C= NP_005364.1:p.Gln118=
XM_011541478.1:c.331C= XP_011539780.1:p.Gln111=
XM_017001320.1:c.523C= XP_016856809.1:p.Gln175=
NM_005373.3:c.352C= MANE Select NP_005364.1:p.Gln118=