Canonical Allele Identifier: CA2645226526

Gene: MPL

Linked Data

• gnomAD v4: 1-43349248-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349253dup , CM000663.2:g.43349253dup	GRCh38
NC_000001.10:g.43814924dup , CM000663.1:g.43814924dup	GRCh37
NC_000001.9:g.43587511dup	NCBI36
NG_007525.1:g.16450dup , LRG_510:g.16450dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1469-10dup MANE Select	ENSP00000361548.3:n.1469-10dup
ENST00000413998.7:c.1448-10dup	ENSP00000414004.3:n.1448-10dup
ENST00000638732.1:n.1469-10dup
ENST00000372470.7:c.1469-10dup	ENSP00000361548.3:n.1469-10dup
ENST00000413998.6:c.1469-10dup	ENSP00000414004.2:n.1469-10dup
ENST00000612993.1:c.1469-10dup	ENSP00000480273.1:n.1469-10dup
NM_005373.2:c.1469-10dup , LRG_510t1:c.1469-10dup	NP_005364.1:n.1469-10dup
XM_011541478.1:c.1448-10dup	XP_011539780.1:n.1448-10dup
XM_017001320.1:c.1640-10dup	XP_016856809.1:n.1640-10dup
NM_005373.3:c.1469-10dup MANE Select	NP_005364.1:n.1469-10dup