Canonical Allele Identifier: CA1139770909

Gene: MPL

Linked Data

• gnomAD v4: 1-43349365-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43349370del , CM000663.2:g.43349370del	GRCh38
NC_000001.10:g.43815041del , CM000663.1:g.43815041del	GRCh37
NC_000001.9:g.43587628del	NCBI36
NG_007525.1:g.16567del , LRG_510:g.16567del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372470.9:c.1565+11del MANE Select	ENSP00000361548.3:n.1565+11del
ENST00000413998.7:c.1544+11del	ENSP00000414004.3:n.1544+11del
ENST00000638732.1:n.1576del
ENST00000643351.1:c.97+11del
ENST00000372470.7:c.1565+11del	ENSP00000361548.3:n.1565+11del
ENST00000413998.6:c.1576del	ENSP00000414004.2:p.Arg526AlafsTer16
ENST00000612993.1:c.1576del	ENSP00000480273.1:p.Arg526AlafsTer24
NM_005373.2:c.1565+11del , LRG_510t1:c.1565+11del	NP_005364.1:n.1565+11del
XM_011541478.1:c.1544+11del	XP_011539780.1:n.1544+11del
XM_017001320.1:c.1736+11del	XP_016856809.1:n.1736+11del
NM_005373.3:c.1565+11del MANE Select	NP_005364.1:n.1565+11del