Canonical Allele Identifier: CA417417419
Gene: MPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.43804300A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338629A>G , CM000663.2:g.43338629A>G GRCh38
NC_000001.10:g.43804300A>G , CM000663.1:g.43804300A>G GRCh37
NC_000001.9:g.43576887A>G NCBI36
NG_007525.1:g.5826A>G , LRG_510:g.5826A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.300A>G MANE Select ENSP00000361548.3:p.Glu100=
ENST00000413998.7:c.279A>G ENSP00000414004.3:p.Glu93=
ENST00000638732.1:n.300A>G
ENST00000372470.7:c.300A>G ENSP00000361548.3:p.Glu100=
ENST00000413998.6:c.300A>G ENSP00000414004.2:p.Glu100=
ENST00000612993.1:c.300A>G ENSP00000480273.1:p.Glu100=
NM_005373.2:c.300A>G , LRG_510t1:c.300A>G NP_005364.1:p.Glu100=
XM_011541478.1:c.279A>G XP_011539780.1:p.Glu93=
XM_017001320.1:c.471A>G XP_016856809.1:p.Glu157=
NM_005373.3:c.300A>G MANE Select NP_005364.1:p.Glu100=