Canonical Allele Identifier: CA339973705
Gene: MPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338657T>A , CM000663.2:g.43338657T>A GRCh38
NC_000001.10:g.43804328T>A , CM000663.1:g.43804328T>A GRCh37
NC_000001.9:g.43576915T>A NCBI36
NG_007525.1:g.5854T>A , LRG_510:g.5854T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.328T>A MANE Select ENSP00000361548.3:p.Trp110Arg
ENST00000413998.7:c.307T>A ENSP00000414004.3:p.Trp103Arg
ENST00000638732.1:n.328T>A
ENST00000372470.7:c.328T>A ENSP00000361548.3:p.Trp110Arg
ENST00000413998.6:c.328T>A ENSP00000414004.2:p.Trp110Arg
ENST00000612993.1:c.328T>A ENSP00000480273.1:p.Trp110Arg
NM_005373.2:c.328T>A , LRG_510t1:c.328T>A NP_005364.1:p.Trp110Arg
XM_011541478.1:c.307T>A XP_011539780.1:p.Trp103Arg
XM_017001320.1:c.499T>A XP_016856809.1:p.Trp167Arg
NM_005373.3:c.328T>A MANE Select NP_005364.1:p.Trp110Arg