Canonical Allele Identifier: CA1165575876
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338100T= , CM000663.2:g.43338100T= GRCh38
NC_000001.10:g.43803771T= , CM000663.1:g.43803771T= GRCh37
NC_000001.9:g.43576358T= NCBI36
NG_007525.1:g.5297T= , LRG_510:g.5297T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.81T= MANE Select ENSP00000361548.3:p.Asp27=
ENST00000413998.7:c.80-20T= ENSP00000414004.3:n.80-20T=
ENST00000638732.1:n.81T=
ENST00000372470.7:c.81T= ENSP00000361548.3:p.Asp27=
ENST00000413998.6:c.81T= ENSP00000414004.2:p.Asp27=
ENST00000612993.1:c.81T= ENSP00000480273.1:p.Asp27=
NM_005373.2:c.81T= , LRG_510t1:c.81T= NP_005364.1:p.Asp27=
XM_011541478.1:c.80-20T= XP_011539780.1:n.80-20T=
XM_017001320.1:c.252T= XP_016856809.1:p.Asp84=
NM_005373.3:c.81T= MANE Select NP_005364.1:p.Asp27=