Canonical Allele Identifier: CA339973432

Gene: MPL

Linked Data

• gnomAD v4: 1-43338595-C-A
• MyVariant Identifiers: chr1:g.43804266C>A (hg19) ; chr1:g.43338595C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338595C>A , CM000663.2:g.43338595C>A	GRCh38
NC_000001.10:g.43804266C>A , CM000663.1:g.43804266C>A	GRCh37
NC_000001.9:g.43576853C>A	NCBI36
NG_007525.1:g.5792C>A , LRG_510:g.5792C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.266C>A MANE Select	ENSP00000361548.3:p.Thr89Asn
ENST00000413998.7:c.245C>A	ENSP00000414004.3:p.Thr82Asn
ENST00000638732.1:n.266C>A
ENST00000372470.7:c.266C>A	ENSP00000361548.3:p.Thr89Asn
ENST00000413998.6:c.266C>A	ENSP00000414004.2:p.Thr89Asn
ENST00000612993.1:c.266C>A	ENSP00000480273.1:p.Thr89Asn
NM_005373.2:c.266C>A , LRG_510t1:c.266C>A	NP_005364.1:p.Thr89Asn
XM_011541478.1:c.245C>A	XP_011539780.1:p.Thr82Asn
XM_017001320.1:c.437C>A	XP_016856809.1:p.Thr146Asn
NM_005373.3:c.266C>A MANE Select	NP_005364.1:p.Thr89Asn