Canonical Allele Identifier: CA2740090647

Gene: MPL

Linked Data

• ClinVar Variation Id: 2924699
• ClinVar RCV Id: RCV003788401

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43337942G>C , CM000663.2:g.43337942G>C	GRCh38
NC_000001.10:g.43803613G>C , CM000663.1:g.43803613G>C	GRCh37
NC_000001.9:g.43576200G>C	NCBI36
NG_007525.1:g.5139G>C , LRG_510:g.5139G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372470.9:c.79+15G>C MANE Select	ENSP00000361548.3:n.79+15G>C
ENST00000413998.7:c.79+15G>C	ENSP00000414004.3:n.79+15G>C
ENST00000638732.1:n.79+15G>C
ENST00000372470.7:c.79+15G>C	ENSP00000361548.3:n.79+15G>C
ENST00000413998.6:c.79+15G>C	ENSP00000414004.2:n.79+15G>C
ENST00000612993.1:c.79+15G>C	ENSP00000480273.1:n.79+15G>C
NM_005373.2:c.79+15G>C , LRG_510t1:c.79+15G>C	NP_005364.1:n.79+15G>C
XM_011541478.1:c.79+15G>C	XP_011539780.1:n.79+15G>C
XM_017001320.1:c.94G>C	XP_016856809.1:p.Gly32Arg
NM_005373.3:c.79+15G>C MANE Select	NP_005364.1:n.79+15G>C