Canonical Allele Identifier: CA339973840

Gene: MPL

Linked Data

• dbSNP Id: rs2153916522
• MyVariant Identifiers: chr1:g.43804345C>G (hg19) ; chr1:g.43338674C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338674C>G , CM000663.2:g.43338674C>G	GRCh38
NC_000001.10:g.43804345C>G , CM000663.1:g.43804345C>G	GRCh37
NC_000001.9:g.43576932C>G	NCBI36
NG_007525.1:g.5871C>G , LRG_510:g.5871C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.345C>G MANE Select	ENSP00000361548.3:p.Phe115Leu
ENST00000413998.7:c.324C>G	ENSP00000414004.3:p.Phe108Leu
ENST00000638732.1:n.345C>G
ENST00000372470.7:c.345C>G	ENSP00000361548.3:p.Phe115Leu
ENST00000413998.6:c.345C>G	ENSP00000414004.2:p.Phe115Leu
ENST00000612993.1:c.345C>G	ENSP00000480273.1:p.Phe115Leu
NM_005373.2:c.345C>G , LRG_510t1:c.345C>G	NP_005364.1:p.Phe115Leu
XM_011541478.1:c.324C>G	XP_011539780.1:p.Phe108Leu
XM_017001320.1:c.516C>G	XP_016856809.1:p.Phe172Leu
NM_005373.3:c.345C>G MANE Select	NP_005364.1:p.Phe115Leu