Canonical Allele Identifier: CA1165576121

Gene: MPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338759_43338760delinsGC , CM000663.2:g.43338759_43338760delinsGC	GRCh38
NC_000001.10:g.43804430_43804431delinsGC , CM000663.1:g.43804430_43804431delinsGC	GRCh37
NC_000001.9:g.43577017_43577018delinsGC	NCBI36
NG_007525.1:g.5956_5957delinsGC , LRG_510:g.5956_5957delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.391+39_391+40delinsGC MANE Select	ENSP00000361548.3:n.391+39_391+40delinsGC
ENST00000413998.7:c.370+39_370+40delinsGC	ENSP00000414004.3:n.370+39_370+40delinsGC
ENST00000638732.1:n.391+39_391+40delinsGC
ENST00000372470.7:c.391+39_391+40delinsGC	ENSP00000361548.3:n.391+39_391+40delinsGC
ENST00000413998.6:c.391+39_391+40delinsGC	ENSP00000414004.2:n.391+39_391+40delinsGC
ENST00000612993.1:c.391+39_391+40delinsGC	ENSP00000480273.1:n.391+39_391+40delinsGC
NM_005373.2:c.391+39_391+40delinsGC , LRG_510t1:c.391+39_391+40delinsGC	NP_005364.1:n.391+39_391+40delinsGC
XM_011541478.1:c.370+39_370+40delinsGC	XP_011539780.1:n.370+39_370+40delinsGC
XM_017001320.1:c.562+39_562+40delinsGC	XP_016856809.1:n.562+39_562+40delinsGC
NM_005373.3:c.391+39_391+40delinsGC MANE Select	NP_005364.1:n.391+39_391+40delinsGC