Canonical Allele Identifier: CA1141580749
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349267G= , CM000663.2:g.43349267G= GRCh38
NC_000001.10:g.43814938G= , CM000663.1:g.43814938G= GRCh37
NC_000001.9:g.43587525G= NCBI36
NG_007525.1:g.16464G= , LRG_510:g.16464G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1473G= MANE Select ENSP00000361548.3:p.Trp491=
ENST00000413998.7:c.1452G= ENSP00000414004.3:p.Trp484=
ENST00000638732.1:n.1473G=
ENST00000643351.1:c.5G=
ENST00000372470.7:c.1473G= ENSP00000361548.3:p.Trp491=
ENST00000413998.6:c.1473G= ENSP00000414004.2:p.Trp491=
ENST00000612993.1:c.1473G= ENSP00000480273.1:p.Trp491=
NM_005373.2:c.1473G= , LRG_510t1:c.1473G= NP_005364.1:p.Trp491=
XM_011541478.1:c.1452G= XP_011539780.1:p.Trp484=
XM_017001320.1:c.1644G= XP_016856809.1:p.Trp548=
NM_005373.3:c.1473G= MANE Select NP_005364.1:p.Trp491=