Canonical Allele Identifier: CA1165576078
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338630G= , CM000663.2:g.43338630G= GRCh38
NC_000001.10:g.43804301G= , CM000663.1:g.43804301G= GRCh37
NC_000001.9:g.43576888G= NCBI36
NG_007525.1:g.5827G= , LRG_510:g.5827G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372470.9:c.301G= MANE Select ENSP00000361548.3:p.Val101=
ENST00000413998.7:c.280G= ENSP00000414004.3:p.Val94=
ENST00000638732.1:n.301G=
ENST00000372470.7:c.301G= ENSP00000361548.3:p.Val101=
ENST00000413998.6:c.301G= ENSP00000414004.2:p.Val101=
ENST00000612993.1:c.301G= ENSP00000480273.1:p.Val101=
NM_005373.2:c.301G= , LRG_510t1:c.301G= NP_005364.1:p.Val101=
XM_011541478.1:c.280G= XP_011539780.1:p.Val94=
XM_017001320.1:c.472G= XP_016856809.1:p.Val158=
NM_005373.3:c.301G= MANE Select NP_005364.1:p.Val101=