Canonical Allele Identifier: CA339988101

Gene: MPL

Linked Data

• gnomAD v4: 1-43349341-A-G
• MyVariant Identifiers: chr1:g.43815012A>G (hg19) ; chr1:g.43349341A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349341A>G , CM000663.2:g.43349341A>G	GRCh38
NC_000001.10:g.43815012A>G , CM000663.1:g.43815012A>G	GRCh37
NC_000001.9:g.43587599A>G	NCBI36
NG_007525.1:g.16538A>G , LRG_510:g.16538A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1547A>G MANE Select	ENSP00000361548.3:p.Gln516Arg
ENST00000413998.7:c.1526A>G	ENSP00000414004.3:p.Gln509Arg
ENST00000638732.1:n.1547A>G
ENST00000643351.1:c.79A>G
ENST00000372470.7:c.1547A>G	ENSP00000361548.3:p.Gln516Arg
ENST00000413998.6:c.1547A>G	ENSP00000414004.2:p.Gln516Arg
ENST00000612993.1:c.1547A>G	ENSP00000480273.1:p.Gln516Arg
NM_005373.2:c.1547A>G , LRG_510t1:c.1547A>G	NP_005364.1:p.Gln516Arg
XM_011541478.1:c.1526A>G	XP_011539780.1:p.Gln509Arg
XM_017001320.1:c.1718A>G	XP_016856809.1:p.Gln573Arg
NM_005373.3:c.1547A>G MANE Select	NP_005364.1:p.Gln516Arg