Canonical Allele Identifier: CA916162769

Gene: MPL

Linked Data

• dbSNP Id: rs1557462747
• gnomAD v4: 1-43338061-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338064del , CM000663.2:g.43338064del	GRCh38
NC_000001.10:g.43803735del , CM000663.1:g.43803735del	GRCh37
NC_000001.9:g.43576322del	NCBI36
NG_007525.1:g.5261del , LRG_510:g.5261del

Transcript Alleles

HGVS	Amino-acid change
ENST00000372470.9:c.80-35del MANE Select	ENSP00000361548.3:n.80-35del
ENST00000413998.7:c.80-56del	ENSP00000414004.3:n.80-56del
ENST00000638732.1:n.80-35del
ENST00000372470.7:c.80-35del	ENSP00000361548.3:n.80-35del
ENST00000413998.6:c.80-35del	ENSP00000414004.2:n.80-35del
ENST00000612993.1:c.80-35del	ENSP00000480273.1:n.80-35del
NM_005373.2:c.80-35del , LRG_510t1:c.80-35del	NP_005364.1:n.80-35del
XM_011541478.1:c.80-56del	XP_011539780.1:n.80-56del
XM_017001320.1:c.216del	XP_016856809.1:p.Arg73GlyfsTer11
NM_005373.3:c.80-35del MANE Select	NP_005364.1:n.80-35del