Canonical Allele Identifier: CA1165576092
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338666A= , CM000663.2:g.43338666A= GRCh38
NC_000001.10:g.43804337A= , CM000663.1:g.43804337A= GRCh37
NC_000001.9:g.43576924A= NCBI36
NG_007525.1:g.5863A= , LRG_510:g.5863A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.337A= MANE Select ENSP00000361548.3:p.Asn113=
ENST00000413998.7:c.316A= ENSP00000414004.3:p.Asn106=
ENST00000638732.1:n.337A=
ENST00000372470.7:c.337A= ENSP00000361548.3:p.Asn113=
ENST00000413998.6:c.337A= ENSP00000414004.2:p.Asn113=
ENST00000612993.1:c.337A= ENSP00000480273.1:p.Asn113=
NM_005373.2:c.337A= , LRG_510t1:c.337A= NP_005364.1:p.Asn113=
XM_011541478.1:c.316A= XP_011539780.1:p.Asn106=
XM_017001320.1:c.508A= XP_016856809.1:p.Asn170=
NM_005373.3:c.337A= MANE Select NP_005364.1:p.Asn113=