Canonical Allele Identifier: CA806556

Gene: MPL

Linked Data

• ClinVar Variation Id: 2934984
• ClinVar RCV Id: RCV003790638
• dbSNP Id: rs778817503
• ExAC: 1:43803615 G / T
• gnomAD v2: 1-43803615-G-T
• gnomAD v4: 1-43337944-G-T
• MyVariant Identifiers: chr1:g.43803615G>T (hg19) ; chr1:g.43337944G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43337944G>T , CM000663.2:g.43337944G>T	GRCh38
NC_000001.10:g.43803615G>T , CM000663.1:g.43803615G>T	GRCh37
NC_000001.9:g.43576202G>T	NCBI36
NG_007525.1:g.5141G>T , LRG_510:g.5141G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.79+17G>T MANE Select	ENSP00000361548.3:n.79+17G>T
ENST00000413998.7:c.79+17G>T	ENSP00000414004.3:n.79+17G>T
ENST00000638732.1:n.79+17G>T
ENST00000372470.7:c.79+17G>T	ENSP00000361548.3:n.79+17G>T
ENST00000413998.6:c.79+17G>T	ENSP00000414004.2:n.79+17G>T
ENST00000612993.1:c.79+17G>T	ENSP00000480273.1:n.79+17G>T
NM_005373.2:c.79+17G>T , LRG_510t1:c.79+17G>T	NP_005364.1:n.79+17G>T
XM_011541478.1:c.79+17G>T	XP_011539780.1:n.79+17G>T
XM_017001320.1:c.96G>T	XP_016856809.1:p.Gly32=
NM_005373.3:c.79+17G>T MANE Select	NP_005364.1:n.79+17G>T