Canonical Allele Identifier: CA339973960

Gene: MPL

Linked Data

• dbSNP Id: rs2153916532
• MyVariant Identifiers: chr1:g.43804364C>G (hg19) ; chr1:g.43338693C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338693C>G , CM000663.2:g.43338693C>G	GRCh38
NC_000001.10:g.43804364C>G , CM000663.1:g.43804364C>G	GRCh37
NC_000001.9:g.43576951C>G	NCBI36
NG_007525.1:g.5890C>G , LRG_510:g.5890C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.364C>G MANE Select	ENSP00000361548.3:p.Gln122Glu
ENST00000413998.7:c.343C>G	ENSP00000414004.3:p.Gln115Glu
ENST00000638732.1:n.364C>G
ENST00000372470.7:c.364C>G	ENSP00000361548.3:p.Gln122Glu
ENST00000413998.6:c.364C>G	ENSP00000414004.2:p.Gln122Glu
ENST00000612993.1:c.364C>G	ENSP00000480273.1:p.Gln122Glu
NM_005373.2:c.364C>G , LRG_510t1:c.364C>G	NP_005364.1:p.Gln122Glu
XM_011541478.1:c.343C>G	XP_011539780.1:p.Gln115Glu
XM_017001320.1:c.535C>G	XP_016856809.1:p.Gln179Glu
NM_005373.3:c.364C>G MANE Select	NP_005364.1:p.Gln122Glu