Canonical Allele Identifier: CA1141867571
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338668T= , CM000663.2:g.43338668T= GRCh38
NC_000001.10:g.43804339T= , CM000663.1:g.43804339T= GRCh37
NC_000001.9:g.43576926T= NCBI36
NG_007525.1:g.5865T= , LRG_510:g.5865T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.339T= MANE Select ENSP00000361548.3:p.Asn113=
ENST00000413998.7:c.318T= ENSP00000414004.3:p.Asn106=
ENST00000638732.1:n.339T=
ENST00000372470.7:c.339T= ENSP00000361548.3:p.Asn113=
ENST00000413998.6:c.339T= ENSP00000414004.2:p.Asn113=
ENST00000612993.1:c.339T= ENSP00000480273.1:p.Asn113=
NM_005373.2:c.339T= , LRG_510t1:c.339T= NP_005364.1:p.Asn113=
XM_011541478.1:c.318T= XP_011539780.1:p.Asn106=
XM_017001320.1:c.510T= XP_016856809.1:p.Asn170=
NM_005373.3:c.339T= MANE Select NP_005364.1:p.Asn113=