Canonical Allele Identifier: CA1165576062

Gene: MPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338595C= , CM000663.2:g.43338595C=	GRCh38
NC_000001.10:g.43804266C= , CM000663.1:g.43804266C=	GRCh37
NC_000001.9:g.43576853C=	NCBI36
NG_007525.1:g.5792C= , LRG_510:g.5792C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.266C= MANE Select	ENSP00000361548.3:p.Thr89=
ENST00000413998.7:c.245C=	ENSP00000414004.3:p.Thr82=
ENST00000638732.1:n.266C=
ENST00000372470.7:c.266C=	ENSP00000361548.3:p.Thr89=
ENST00000413998.6:c.266C=	ENSP00000414004.2:p.Thr89=
ENST00000612993.1:c.266C=	ENSP00000480273.1:p.Thr89=
NM_005373.2:c.266C= , LRG_510t1:c.266C=	NP_005364.1:p.Thr89=
XM_011541478.1:c.245C=	XP_011539780.1:p.Thr82=
XM_017001320.1:c.437C=	XP_016856809.1:p.Thr146=
NM_005373.3:c.266C= MANE Select	NP_005364.1:p.Thr89=