Canonical Allele Identifier: CA1142381939
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338590T= , CM000663.2:g.43338590T= GRCh38
NC_000001.10:g.43804261T= , CM000663.1:g.43804261T= GRCh37
NC_000001.9:g.43576848T= NCBI36
NG_007525.1:g.5787T= , LRG_510:g.5787T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.261T= MANE Select ENSP00000361548.3:p.Phe87=
ENST00000413998.7:c.240T= ENSP00000414004.3:p.Phe80=
ENST00000638732.1:n.261T=
ENST00000372470.7:c.261T= ENSP00000361548.3:p.Phe87=
ENST00000413998.6:c.261T= ENSP00000414004.2:p.Phe87=
ENST00000612993.1:c.261T= ENSP00000480273.1:p.Phe87=
NM_005373.2:c.261T= , LRG_510t1:c.261T= NP_005364.1:p.Phe87=
XM_011541478.1:c.240T= XP_011539780.1:p.Phe80=
XM_017001320.1:c.432T= XP_016856809.1:p.Phe144=
NM_005373.3:c.261T= MANE Select NP_005364.1:p.Phe87=