Canonical Allele Identifier: CA2695806192
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs2153916474

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338615_43338616insTTCT , CM000663.2:g.43338615_43338616insTTCT GRCh38
NC_000001.10:g.43804286_43804287insTTCT , CM000663.1:g.43804286_43804287insTTCT GRCh37
NC_000001.9:g.43576873_43576874insTTCT NCBI36
NG_007525.1:g.5812_5813insTTCT , LRG_510:g.5812_5813insTTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.286_287insTTCT MANE Select ENSP00000361548.3:p.Pro96LeufsTer?
ENST00000413998.7:c.265_266insTTCT ENSP00000414004.3:p.Pro89LeufsTer?
ENST00000638732.1:n.286_287insTTCT
ENST00000372470.7:c.286_287insTTCT ENSP00000361548.3:p.Pro96LeufsTer?
ENST00000413998.6:c.286_287insTTCT ENSP00000414004.2:p.Pro96LeufsTer?
ENST00000612993.1:c.286_287insTTCT ENSP00000480273.1:p.Pro96LeufsTer?
NM_005373.2:c.286_287insTTCT , LRG_510t1:c.286_287insTTCT NP_005364.1:p.Pro96LeufsTer?
XM_011541478.1:c.265_266insTTCT XP_011539780.1:p.Pro89LeufsTer?
XM_017001320.1:c.457_458insTTCT XP_016856809.1:p.Pro153LeufsTer?
NM_005373.3:c.286_287insTTCT MANE Select NP_005364.1:p.Pro96LeufsTer?