Canonical Allele Identifier: CA339973995

Gene: MPL

Linked Data

• MyVariant Identifiers: chr1:g.43804371T>A (hg19) ; chr1:g.43338700T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338700T>A , CM000663.2:g.43338700T>A	GRCh38
NC_000001.10:g.43804371T>A , CM000663.1:g.43804371T>A	GRCh37
NC_000001.9:g.43576958T>A	NCBI36
NG_007525.1:g.5897T>A , LRG_510:g.5897T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.371T>A MANE Select	ENSP00000361548.3:p.Val124Asp
ENST00000413998.7:c.350T>A	ENSP00000414004.3:p.Val117Asp
ENST00000638732.1:n.371T>A
ENST00000372470.7:c.371T>A	ENSP00000361548.3:p.Val124Asp
ENST00000413998.6:c.371T>A	ENSP00000414004.2:p.Val124Asp
ENST00000612993.1:c.371T>A	ENSP00000480273.1:p.Val124Asp
NM_005373.2:c.371T>A , LRG_510t1:c.371T>A	NP_005364.1:p.Val124Asp
XM_011541478.1:c.350T>A	XP_011539780.1:p.Val117Asp
XM_017001320.1:c.542T>A	XP_016856809.1:p.Val181Asp
NM_005373.3:c.371T>A MANE Select	NP_005364.1:p.Val124Asp