Canonical Allele Identifier: CA2740090672

Gene: MPL

Linked Data

• ClinVar Variation Id: 2929179
• ClinVar RCV Id: RCV003781905

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349378dup , CM000663.2:g.43349378dup	GRCh38
NC_000001.10:g.43815049dup , CM000663.1:g.43815049dup	GRCh37
NC_000001.9:g.43587636dup	NCBI36
NG_007525.1:g.16575dup , LRG_510:g.16575dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1565+19dup MANE Select	ENSP00000361548.3:n.1565+19dup
ENST00000413998.7:c.1544+19dup	ENSP00000414004.3:n.1544+19dup
ENST00000638732.1:n.1584dup
ENST00000643351.1:c.97+19dup
ENST00000372470.7:c.1565+19dup	ENSP00000361548.3:n.1565+19dup
ENST00000413998.6:c.1584dup	ENSP00000414004.2:p.Gly529ArgfsTer?
ENST00000612993.1:c.1584dup	ENSP00000480273.1:p.Gly529ArgfsTer13
NM_005373.2:c.1565+19dup , LRG_510t1:c.1565+19dup	NP_005364.1:n.1565+19dup
XM_011541478.1:c.1544+19dup	XP_011539780.1:n.1544+19dup
XM_017001320.1:c.1736+19dup	XP_016856809.1:n.1736+19dup
NM_005373.3:c.1565+19dup MANE Select	NP_005364.1:n.1565+19dup