Canonical Allele Identifier: CA2580062777

Gene: MPL

Linked Data

• ClinVar Variation Id: 2024771
• ClinVar RCV Id: RCV002847942

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43338082C>T , CM000663.2:g.43338082C>T	GRCh38
NC_000001.10:g.43803753C>T , CM000663.1:g.43803753C>T	GRCh37
NC_000001.9:g.43576340C>T	NCBI36
NG_007525.1:g.5279C>T , LRG_510:g.5279C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.80-17C>T MANE Select	ENSP00000361548.3:n.80-17C>T
ENST00000413998.7:c.80-38C>T	ENSP00000414004.3:n.80-38C>T
ENST00000638732.1:n.80-17C>T
ENST00000372470.7:c.80-17C>T	ENSP00000361548.3:n.80-17C>T
ENST00000413998.6:c.80-17C>T	ENSP00000414004.2:n.80-17C>T
ENST00000612993.1:c.80-17C>T	ENSP00000480273.1:n.80-17C>T
NM_005373.2:c.80-17C>T , LRG_510t1:c.80-17C>T	NP_005364.1:n.80-17C>T
XM_011541478.1:c.80-38C>T	XP_011539780.1:n.80-38C>T
XM_017001320.1:c.234C>T	XP_016856809.1:p.Leu78=
NM_005373.3:c.80-17C>T MANE Select	NP_005364.1:n.80-17C>T