Canonical Allele Identifier: CA339973373
Gene: MPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338571C>A , CM000663.2:g.43338571C>A GRCh38
NC_000001.10:g.43804242C>A , CM000663.1:g.43804242C>A GRCh37
NC_000001.9:g.43576829C>A NCBI36
NG_007525.1:g.5768C>A , LRG_510:g.5768C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.242C>A MANE Select ENSP00000361548.3:p.Ser81Tyr
ENST00000413998.7:c.221C>A ENSP00000414004.3:p.Ser74Tyr
ENST00000638732.1:n.242C>A
ENST00000372470.7:c.242C>A ENSP00000361548.3:p.Ser81Tyr
ENST00000413998.6:c.242C>A ENSP00000414004.2:p.Ser81Tyr
ENST00000612993.1:c.242C>A ENSP00000480273.1:p.Ser81Tyr
NM_005373.2:c.242C>A , LRG_510t1:c.242C>A NP_005364.1:p.Ser81Tyr
XM_011541478.1:c.221C>A XP_011539780.1:p.Ser74Tyr
XM_017001320.1:c.413C>A XP_016856809.1:p.Ser138Tyr
NM_005373.3:c.242C>A MANE Select NP_005364.1:p.Ser81Tyr