Canonical Allele Identifier: CA1165579823

Gene: MPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349227_43349233delinsCGGGTGG , CM000663.2:g.43349227_43349233delinsCGGGTGG	GRCh38
NC_000001.10:g.43814898_43814904delinsCGGGTGG , CM000663.1:g.43814898_43814904delinsCGGGTGG	GRCh37
NC_000001.9:g.43587485_43587491delinsCGGGTGG	NCBI36
NG_007525.1:g.16424_16430delinsCGGGTGG , LRG_510:g.16424_16430delinsCGGGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1469-36_1469-30delinsCGGGTGG MANE Select	ENSP00000361548.3:n.1469-36_1469-30delinsCGGGTGG
ENST00000413998.7:c.1448-36_1448-30delinsCGGGTGG	ENSP00000414004.3:n.1448-36_1448-30delinsCGGGTGG
ENST00000638732.1:n.1469-36_1469-30delinsCGGGTGG
ENST00000372470.7:c.1469-36_1469-30delinsCGGGTGG	ENSP00000361548.3:n.1469-36_1469-30delinsCGGGTGG
ENST00000413998.6:c.1469-36_1469-30delinsCGGGTGG	ENSP00000414004.2:n.1469-36_1469-30delinsCGGGTGG
ENST00000612993.1:c.1469-36_1469-30delinsCGGGTGG	ENSP00000480273.1:n.1469-36_1469-30delinsCGGGTGG
NM_005373.2:c.1469-36_1469-30delinsCGGGTGG , LRG_510t1:c.1469-36_1469-30delinsCGGGTGG	NP_005364.1:n.1469-36_1469-30delinsCGGGTGG
XM_011541478.1:c.1448-36_1448-30delinsCGGGTGG	XP_011539780.1:n.1448-36_1448-30delinsCGGGTGG
XM_017001320.1:c.1640-36_1640-30delinsCGGGTGG	XP_016856809.1:n.1640-36_1640-30delinsCGGGTGG
NM_005373.3:c.1469-36_1469-30delinsCGGGTGG MANE Select	NP_005364.1:n.1469-36_1469-30delinsCGGGTGG