Canonical Allele Identifier: CA1165575812

Gene: MPL

Linked Data

• dbSNP Id: rs1647005058
• gnomAD v4: 1-43337938-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43337938C>G , CM000663.2:g.43337938C>G	GRCh38
NC_000001.10:g.43803609C>G , CM000663.1:g.43803609C>G	GRCh37
NC_000001.9:g.43576196C>G	NCBI36
NG_007525.1:g.5135C>G , LRG_510:g.5135C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.79+11C>G MANE Select	ENSP00000361548.3:n.79+11C>G
ENST00000413998.7:c.79+11C>G	ENSP00000414004.3:n.79+11C>G
ENST00000638732.1:n.79+11C>G
ENST00000372470.7:c.79+11C>G	ENSP00000361548.3:n.79+11C>G
ENST00000413998.6:c.79+11C>G	ENSP00000414004.2:n.79+11C>G
ENST00000612993.1:c.79+11C>G	ENSP00000480273.1:n.79+11C>G
NM_005373.2:c.79+11C>G , LRG_510t1:c.79+11C>G	NP_005364.1:n.79+11C>G
XM_011541478.1:c.79+11C>G	XP_011539780.1:n.79+11C>G
XM_017001320.1:c.90C>G	XP_016856809.1:p.His30Gln
NM_005373.3:c.79+11C>G MANE Select	NP_005364.1:n.79+11C>G