Canonical Allele Identifier: CA1165576072
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338618G= , CM000663.2:g.43338618G= GRCh38
NC_000001.10:g.43804289G= , CM000663.1:g.43804289G= GRCh37
NC_000001.9:g.43576876G= NCBI36
NG_007525.1:g.5815G= , LRG_510:g.5815G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.289G= MANE Select ENSP00000361548.3:p.Asp97=
ENST00000413998.7:c.268G= ENSP00000414004.3:p.Asp90=
ENST00000638732.1:n.289G=
ENST00000372470.7:c.289G= ENSP00000361548.3:p.Asp97=
ENST00000413998.6:c.289G= ENSP00000414004.2:p.Asp97=
ENST00000612993.1:c.289G= ENSP00000480273.1:p.Asp97=
NM_005373.2:c.289G= , LRG_510t1:c.289G= NP_005364.1:p.Asp97=
XM_011541478.1:c.268G= XP_011539780.1:p.Asp90=
XM_017001320.1:c.460G= XP_016856809.1:p.Asp154=
NM_005373.3:c.289G= MANE Select NP_005364.1:p.Asp97=