Canonical Allele Identifier: CA1148224237
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338592G= , CM000663.2:g.43338592G= GRCh38
NC_000001.10:g.43804263G= , CM000663.1:g.43804263G= GRCh37
NC_000001.9:g.43576850G= NCBI36
NG_007525.1:g.5789G= , LRG_510:g.5789G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.263G= MANE Select ENSP00000361548.3:p.Gly88=
ENST00000413998.7:c.242G= ENSP00000414004.3:p.Gly81=
ENST00000638732.1:n.263G=
ENST00000372470.7:c.263G= ENSP00000361548.3:p.Gly88=
ENST00000413998.6:c.263G= ENSP00000414004.2:p.Gly88=
ENST00000612993.1:c.263G= ENSP00000480273.1:p.Gly88=
NM_005373.2:c.263G= , LRG_510t1:c.263G= NP_005364.1:p.Gly88=
XM_011541478.1:c.242G= XP_011539780.1:p.Gly81=
XM_017001320.1:c.434G= XP_016856809.1:p.Gly145=
NM_005373.3:c.263G= MANE Select NP_005364.1:p.Gly88=