Canonical Allele Identifier: CA339995083

Gene: MPL

Linked Data

• MyVariant Identifiers: chr1:g.43818439C>G (hg19) ; chr1:g.43352768C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43352768C>G , CM000663.2:g.43352768C>G	GRCh38
NC_000001.10:g.43818439C>G , CM000663.1:g.43818439C>G	GRCh37
NC_000001.9:g.43591026C>G	NCBI36
NG_007525.1:g.19965C>G , LRG_510:g.19965C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000372470.9:c.1904C>G MANE Select	ENSP00000361548.3:p.Pro635Arg
ENST00000413998.7:c.1883C>G	ENSP00000414004.3:p.Pro628Arg
ENST00000372470.7:c.1904C>G	ENSP00000361548.3:p.Pro635Arg
NM_005373.2:c.1904C>G , LRG_510t1:c.1904C>G	NP_005364.1:p.Pro635Arg
XM_011541478.1:c.1883C>G	XP_011539780.1:p.Pro628Arg
XM_017001320.1:c.2075C>G	XP_016856809.1:p.Pro692Arg
NM_005373.3:c.1904C>G MANE Select	NP_005364.1:p.Pro635Arg