Canonical Allele Identifier: CA339973963

Gene: MPL

Linked Data

• MyVariant Identifiers: chr1:g.43804364C>T (hg19) ; chr1:g.43338693C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338693C>T , CM000663.2:g.43338693C>T	GRCh38
NC_000001.10:g.43804364C>T , CM000663.1:g.43804364C>T	GRCh37
NC_000001.9:g.43576951C>T	NCBI36
NG_007525.1:g.5890C>T , LRG_510:g.5890C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.364C>T MANE Select	ENSP00000361548.3:p.Gln122Ter
ENST00000413998.7:c.343C>T	ENSP00000414004.3:p.Gln115Ter
ENST00000638732.1:n.364C>T
ENST00000372470.7:c.364C>T	ENSP00000361548.3:p.Gln122Ter
ENST00000413998.6:c.364C>T	ENSP00000414004.2:p.Gln122Ter
ENST00000612993.1:c.364C>T	ENSP00000480273.1:p.Gln122Ter
NM_005373.2:c.364C>T , LRG_510t1:c.364C>T	NP_005364.1:p.Gln122Ter
XM_011541478.1:c.343C>T	XP_011539780.1:p.Gln115Ter
XM_017001320.1:c.535C>T	XP_016856809.1:p.Gln179Ter
NM_005373.3:c.364C>T MANE Select	NP_005364.1:p.Gln122Ter