Canonical Allele Identifier: CA1165575990

Gene: MPL

Linked Data

• dbSNP Id: rs1647008620

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338392_43338393insA , CM000663.2:g.43338392_43338393insA	GRCh38
NC_000001.10:g.43804063_43804064insA , CM000663.1:g.43804063_43804064insA	GRCh37
NC_000001.9:g.43576650_43576651insA	NCBI36
NG_007525.1:g.5589_5590insA , LRG_510:g.5589_5590insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.213-150_213-149insA MANE Select	ENSP00000361548.3:n.213-150_213-149insA
ENST00000413998.7:c.192-150_192-149insA	ENSP00000414004.3:n.192-150_192-149insA
ENST00000638732.1:n.213-150_213-149insA
ENST00000372470.7:c.213-150_213-149insA	ENSP00000361548.3:n.213-150_213-149insA
ENST00000413998.6:c.213-150_213-149insA	ENSP00000414004.2:n.213-150_213-149insA
ENST00000612993.1:c.213-150_213-149insA	ENSP00000480273.1:n.213-150_213-149insA
NM_005373.2:c.213-150_213-149insA , LRG_510t1:c.213-150_213-149insA	NP_005364.1:n.213-150_213-149insA
XM_011541478.1:c.192-150_192-149insA	XP_011539780.1:n.192-150_192-149insA
XM_017001320.1:c.384-150_384-149insA	XP_016856809.1:n.384-150_384-149insA
NM_005373.3:c.213-150_213-149insA MANE Select	NP_005364.1:n.213-150_213-149insA