Canonical Allele Identifier: CA417428396

Gene: MPL

Linked Data

• MyVariant Identifiers: chr1:g.43818347G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43352676G>T , CM000663.2:g.43352676G>T	GRCh38
NC_000001.10:g.43818347G>T , CM000663.1:g.43818347G>T	GRCh37
NC_000001.9:g.43590934G>T	NCBI36
NG_007525.1:g.19873G>T , LRG_510:g.19873G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000372470.9:c.1812G>T MANE Select	ENSP00000361548.3:p.Leu604=
ENST00000413998.7:c.1791G>T	ENSP00000414004.3:p.Leu597=
ENST00000643351.1:c.470G>T
ENST00000372470.7:c.1812G>T	ENSP00000361548.3:p.Leu604=
NM_005373.2:c.1812G>T , LRG_510t1:c.1812G>T	NP_005364.1:p.Leu604=
XM_011541478.1:c.1791G>T	XP_011539780.1:p.Leu597=
XM_017001320.1:c.1983G>T	XP_016856809.1:p.Leu661=
NM_005373.3:c.1812G>T MANE Select	NP_005364.1:p.Leu604=