Canonical Allele Identifier: CA645528775

Gene: MPL

Linked Data

• COSMIC: COSM29009

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349336_43349338delinsAGC , CM000663.2:g.43349336_43349338delinsAGC	GRCh38
NC_000001.10:g.43815007_43815009delinsAGC , CM000663.1:g.43815007_43815009delinsAGC	GRCh37
NC_000001.9:g.43587594_43587596delinsAGC	NCBI36
NG_007525.1:g.16533_16535delinsAGC , LRG_510:g.16533_16535delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1542_1544delinsAGC MANE Select	ENSP00000361548.3:p.Trp515Ala
ENST00000413998.7:c.1521_1523delinsAGC	ENSP00000414004.3:p.Trp508Ala
ENST00000638732.1:n.1542_1544delinsAGC
ENST00000643351.1:c.74_76delinsAGC
ENST00000372470.7:c.1542_1544delinsAGC	ENSP00000361548.3:p.Trp515Ala
ENST00000413998.6:c.1542_1544delinsAGC	ENSP00000414004.2:p.Trp515Ala
ENST00000612993.1:c.1542_1544delinsAGC	ENSP00000480273.1:p.Trp515Ala
NM_005373.2:c.1542_1544delinsAGC , LRG_510t1:c.1542_1544delinsAGC	NP_005364.1:p.Trp515Ala
XM_011541478.1:c.1521_1523delinsAGC	XP_011539780.1:p.Trp508Ala
XM_017001320.1:c.1713_1715delinsAGC	XP_016856809.1:p.Trp572Ala
NM_005373.3:c.1542_1544delinsAGC MANE Select	NP_005364.1:p.Trp515Ala