Canonical Allele Identifier: CA1165576104
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs587778515

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338707dup , CM000663.2:g.43338707dup GRCh38
NC_000001.10:g.43804378dup , CM000663.1:g.43804378dup GRCh37
NC_000001.9:g.43576965dup NCBI36
NG_007525.1:g.5904dup , LRG_510:g.5904dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.378dup MANE Select ENSP00000361548.3:p.Val127CysfsTer?
ENST00000413998.7:c.357dup ENSP00000414004.3:p.Val120CysfsTer?
ENST00000638732.1:n.378dup
ENST00000372470.7:c.378dup ENSP00000361548.3:p.Val127CysfsTer?
ENST00000413998.6:c.378dup ENSP00000414004.2:p.Val127CysfsTer?
ENST00000612993.1:c.378dup ENSP00000480273.1:p.Val127CysfsTer?
NM_005373.2:c.378dup , LRG_510t1:c.378dup NP_005364.1:p.Val127CysfsTer?
XM_011541478.1:c.357dup XP_011539780.1:p.Val120CysfsTer?
XM_017001320.1:c.549dup XP_016856809.1:p.Val184CysfsTer?
NM_005373.3:c.378dup MANE Select NP_005364.1:p.Val127CysfsTer?