Canonical Allele Identifier: CA339987622

Gene: MPL

Linked Data

• MyVariant Identifiers: chr1:g.43814967T>A (hg19) ; chr1:g.43349296T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349296T>A , CM000663.2:g.43349296T>A	GRCh38
NC_000001.10:g.43814967T>A , CM000663.1:g.43814967T>A	GRCh37
NC_000001.9:g.43587554T>A	NCBI36
NG_007525.1:g.16493T>A , LRG_510:g.16493T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1502T>A MANE Select	ENSP00000361548.3:p.Val501Glu
ENST00000413998.7:c.1481T>A	ENSP00000414004.3:p.Val494Glu
ENST00000638732.1:n.1502T>A
ENST00000643351.1:c.34T>A
ENST00000372470.7:c.1502T>A	ENSP00000361548.3:p.Val501Glu
ENST00000413998.6:c.1502T>A	ENSP00000414004.2:p.Val501Glu
ENST00000612993.1:c.1502T>A	ENSP00000480273.1:p.Val501Glu
NM_005373.2:c.1502T>A , LRG_510t1:c.1502T>A	NP_005364.1:p.Val501Glu
XM_011541478.1:c.1481T>A	XP_011539780.1:p.Val494Glu
XM_017001320.1:c.1673T>A	XP_016856809.1:p.Val558Glu
NM_005373.3:c.1502T>A MANE Select	NP_005364.1:p.Val501Glu