Canonical Allele Identifier: CA2645222460

Gene: MPL

Linked Data

• gnomAD v4: 1-43338722-T-TAAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338723_43338726dup , CM000663.2:g.43338723_43338726dup	GRCh38
NC_000001.10:g.43804394_43804397dup , CM000663.1:g.43804394_43804397dup	GRCh37
NC_000001.9:g.43576981_43576984dup	NCBI36
NG_007525.1:g.5920_5923dup , LRG_510:g.5920_5923dup

Transcript Alleles

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