Canonical Allele Identifier: CA339973032
Community Standard Title: NM_005373.3(MPL):c.189C>G (p.Tyr63Ter)
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338208C>G , CM000663.2:g.43338208C>G GRCh38
NC_000001.10:g.43803879C>G , CM000663.1:g.43803879C>G GRCh37
NC_000001.9:g.43576466C>G NCBI36
NG_007525.1:g.5405C>G , LRG_510:g.5405C>G

Transcript Alleles

HGVS Amino-acid Change
NM_005373.3:c.189C>G MANE Select NP_005364.1:p.Tyr63Ter
ENST00000372470.9:c.189C>G MANE Select ENSP00000361548.3:p.Tyr63Ter
NM_005373.2:c.189C>G , LRG_510t1:c.189C>G NP_005364.1:p.Tyr63Ter
ENST00000372470.7:c.189C>G ENSP00000361548.3:p.Tyr63Ter
ENST00000413998.6:c.189C>G ENSP00000414004.2:p.Tyr63Ter
ENST00000413998.7:c.168C>G ENSP00000414004.3:p.Tyr56Ter
ENST00000612993.1:c.189C>G ENSP00000480273.1:p.Tyr63Ter
ENST00000638732.1:n.189C>G
XM_011541478.1:c.168C>G XP_011539780.1:p.Tyr56Ter
XM_017001320.1:c.360C>G XP_016856809.1:p.Tyr120Ter