Canonical Allele Identifier: CA339973407
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs773339670

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338583C>T , CM000663.2:g.43338583C>T GRCh38
NC_000001.10:g.43804254C>T , CM000663.1:g.43804254C>T GRCh37
NC_000001.9:g.43576841C>T NCBI36
NG_007525.1:g.5780C>T , LRG_510:g.5780C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.254C>T MANE Select ENSP00000361548.3:p.Pro85Leu
ENST00000413998.7:c.233C>T ENSP00000414004.3:p.Pro78Leu
ENST00000638732.1:n.254C>T
ENST00000372470.7:c.254C>T ENSP00000361548.3:p.Pro85Leu
ENST00000413998.6:c.254C>T ENSP00000414004.2:p.Pro85Leu
ENST00000612993.1:c.254C>T ENSP00000480273.1:p.Pro85Leu
NM_005373.2:c.254C>T , LRG_510t1:c.254C>T NP_005364.1:p.Pro85Leu
XM_011541478.1:c.233C>T XP_011539780.1:p.Pro78Leu
XM_017001320.1:c.425C>T XP_016856809.1:p.Pro142Leu
NM_005373.3:c.254C>T MANE Select NP_005364.1:p.Pro85Leu