Canonical Allele Identifier: CA1165575962

Gene: MPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338356_43338357delinsGA , CM000663.2:g.43338356_43338357delinsGA	GRCh38
NC_000001.10:g.43804027_43804028delinsGA , CM000663.1:g.43804027_43804028delinsGA	GRCh37
NC_000001.9:g.43576614_43576615delinsGA	NCBI36
NG_007525.1:g.5553_5554delinsGA , LRG_510:g.5553_5554delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.212+125_212+126delinsGA MANE Select	ENSP00000361548.3:n.212+125_212+126delinsGA
ENST00000413998.7:c.191+125_191+126delinsGA	ENSP00000414004.3:n.191+125_191+126delinsGA
ENST00000638732.1:n.212+125_212+126delinsGA
ENST00000372470.7:c.212+125_212+126delinsGA	ENSP00000361548.3:n.212+125_212+126delinsGA
ENST00000413998.6:c.212+125_212+126delinsGA	ENSP00000414004.2:n.212+125_212+126delinsGA
ENST00000612993.1:c.212+125_212+126delinsGA	ENSP00000480273.1:n.212+125_212+126delinsGA
NM_005373.2:c.212+125_212+126delinsGA , LRG_510t1:c.212+125_212+126delinsGA	NP_005364.1:n.212+125_212+126delinsGA
XM_011541478.1:c.191+125_191+126delinsGA	XP_011539780.1:n.191+125_191+126delinsGA
XM_017001320.1:c.383+125_383+126delinsGA	XP_016856809.1:n.383+125_383+126delinsGA
NM_005373.3:c.212+125_212+126delinsGA MANE Select	NP_005364.1:n.212+125_212+126delinsGA