Canonical Allele Identifier: CA1165575981

Gene: MPL

Linked Data

• dbSNP Id: rs1647008516

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338378_43338384del , CM000663.2:g.43338378_43338384del	GRCh38
NC_000001.10:g.43804049_43804055del , CM000663.1:g.43804049_43804055del	GRCh37
NC_000001.9:g.43576636_43576642del	NCBI36
NG_007525.1:g.5575_5581del , LRG_510:g.5575_5581del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.212+147_212+153del MANE Select	ENSP00000361548.3:n.212+147_212+153del
ENST00000413998.7:c.191+147_191+153del	ENSP00000414004.3:n.191+147_191+153del
ENST00000638732.1:n.212+147_212+153del
ENST00000372470.7:c.212+147_212+153del	ENSP00000361548.3:n.212+147_212+153del
ENST00000413998.6:c.212+147_212+153del	ENSP00000414004.2:n.212+147_212+153del
ENST00000612993.1:c.212+147_212+153del	ENSP00000480273.1:n.212+147_212+153del
NM_005373.2:c.212+147_212+153del , LRG_510t1:c.212+147_212+153del	NP_005364.1:n.212+147_212+153del
XM_011541478.1:c.191+147_191+153del	XP_011539780.1:n.191+147_191+153del
XM_017001320.1:c.383+147_383+153del	XP_016856809.1:n.383+147_383+153del
NM_005373.3:c.212+147_212+153del MANE Select	NP_005364.1:n.212+147_212+153del