Canonical Allele Identifier: CA339974139

Gene: MPL

Linked Data

• MyVariant Identifiers: chr1:g.43804391G>T (hg19) ; chr1:g.43338720G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338720G>T , CM000663.2:g.43338720G>T	GRCh38
NC_000001.10:g.43804391G>T , CM000663.1:g.43804391G>T	GRCh37
NC_000001.9:g.43576978G>T	NCBI36
NG_007525.1:g.5917G>T , LRG_510:g.5917G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.391G>T MANE Select	ENSP00000361548.3:p.Gly131Cys
ENST00000413998.7:c.370G>T	ENSP00000414004.3:p.Gly124Cys
ENST00000638732.1:n.391G>T
ENST00000372470.7:c.391G>T	ENSP00000361548.3:p.Gly131Cys
ENST00000413998.6:c.391G>T	ENSP00000414004.2:p.Gly131Cys
ENST00000612993.1:c.391G>T	ENSP00000480273.1:p.Gly131Cys
NM_005373.2:c.391G>T , LRG_510t1:c.391G>T	NP_005364.1:p.Gly131Cys
XM_011541478.1:c.370G>T	XP_011539780.1:p.Gly124Cys
XM_017001320.1:c.562G>T	XP_016856809.1:p.Gly188Cys
NM_005373.3:c.391G>T MANE Select	NP_005364.1:p.Gly131Cys