Canonical Allele Identifier: CA1165576089
Gene: MPL HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.328T= MANE Select ENSP00000361548.3:p.Trp110=
ENST00000413998.7:c.307T= ENSP00000414004.3:p.Trp103=
ENST00000638732.1:n.328T=
ENST00000372470.7:c.328T= ENSP00000361548.3:p.Trp110=
ENST00000413998.6:c.328T= ENSP00000414004.2:p.Trp110=
ENST00000612993.1:c.328T= ENSP00000480273.1:p.Trp110=
NM_005373.2:c.328T= , LRG_510t1:c.328T= NP_005364.1:p.Trp110=
XM_011541478.1:c.307T= XP_011539780.1:p.Trp103=
XM_017001320.1:c.499T= XP_016856809.1:p.Trp167=
NM_005373.3:c.328T= MANE Select NP_005364.1:p.Trp110=