Canonical Allele Identifier: CA806628
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338602C>T , CM000663.2:g.43338602C>T GRCh38
NC_000001.10:g.43804273C>T , CM000663.1:g.43804273C>T GRCh37
NC_000001.9:g.43576860C>T NCBI36
NG_007525.1:g.5799C>T , LRG_510:g.5799C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.273C>T MANE Select ENSP00000361548.3:p.Tyr91=
ENST00000413998.7:c.252C>T ENSP00000414004.3:p.Tyr84=
ENST00000638732.1:n.273C>T
ENST00000372470.7:c.273C>T ENSP00000361548.3:p.Tyr91=
ENST00000413998.6:c.273C>T ENSP00000414004.2:p.Tyr91=
ENST00000612993.1:c.273C>T ENSP00000480273.1:p.Tyr91=
NM_005373.2:c.273C>T , LRG_510t1:c.273C>T NP_005364.1:p.Tyr91=
XM_011541478.1:c.252C>T XP_011539780.1:p.Tyr84=
XM_017001320.1:c.444C>T XP_016856809.1:p.Tyr148=
NM_005373.3:c.273C>T MANE Select NP_005364.1:p.Tyr91=