Canonical Allele Identifier: CA339973391
Gene: MPL HGNC NCBI

Linked Data

gnomAD v4: 1-43338576-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338576A>G , CM000663.2:g.43338576A>G GRCh38
NC_000001.10:g.43804247A>G , CM000663.1:g.43804247A>G GRCh37
NC_000001.9:g.43576834A>G NCBI36
NG_007525.1:g.5773A>G , LRG_510:g.5773A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.247A>G MANE Select ENSP00000361548.3:p.Ser83Gly
ENST00000413998.7:c.226A>G ENSP00000414004.3:p.Ser76Gly
ENST00000638732.1:n.247A>G
ENST00000372470.7:c.247A>G ENSP00000361548.3:p.Ser83Gly
ENST00000413998.6:c.247A>G ENSP00000414004.2:p.Ser83Gly
ENST00000612993.1:c.247A>G ENSP00000480273.1:p.Ser83Gly
NM_005373.2:c.247A>G , LRG_510t1:c.247A>G NP_005364.1:p.Ser83Gly
XM_011541478.1:c.226A>G XP_011539780.1:p.Ser76Gly
XM_017001320.1:c.418A>G XP_016856809.1:p.Ser140Gly
NM_005373.3:c.247A>G MANE Select NP_005364.1:p.Ser83Gly