Canonical Allele Identifier: CA1140495612
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338634G= , CM000663.2:g.43338634G= GRCh38
NC_000001.10:g.43804305G= , CM000663.1:g.43804305G= GRCh37
NC_000001.9:g.43576892G= NCBI36
NG_007525.1:g.5831G= , LRG_510:g.5831G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.305G= MANE Select ENSP00000361548.3:p.Arg102=
ENST00000413998.7:c.284G= ENSP00000414004.3:p.Arg95=
ENST00000638732.1:n.305G=
ENST00000372470.7:c.305G= ENSP00000361548.3:p.Arg102=
ENST00000413998.6:c.305G= ENSP00000414004.2:p.Arg102=
ENST00000612993.1:c.305G= ENSP00000480273.1:p.Arg102=
NM_005373.2:c.305G= , LRG_510t1:c.305G= NP_005364.1:p.Arg102=
XM_011541478.1:c.284G= XP_011539780.1:p.Arg95=
XM_017001320.1:c.476G= XP_016856809.1:p.Arg159=
NM_005373.3:c.305G= MANE Select NP_005364.1:p.Arg102=