Canonical Allele Identifier: CA417546719
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43339299G>A , CM000663.2:g.43339299G>A GRCh38
NC_000001.10:g.43804970G>A , CM000663.1:g.43804970G>A GRCh37
NC_000001.9:g.43577557G>A NCBI36
NG_007525.1:g.6496G>A , LRG_510:g.6496G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.420G>A MANE Select ENSP00000361548.3:p.Lys140=
ENST00000413998.7:c.399G>A ENSP00000414004.3:p.Lys133=
ENST00000638732.1:n.420G>A
ENST00000372470.7:c.420G>A ENSP00000361548.3:p.Lys140=
ENST00000413998.6:c.420G>A ENSP00000414004.2:p.Lys140=
ENST00000612993.1:c.420G>A ENSP00000480273.1:p.Lys140=
NM_005373.2:c.420G>A , LRG_510t1:c.420G>A NP_005364.1:p.Lys140=
XM_011541478.1:c.399G>A XP_011539780.1:p.Lys133=
XM_017001320.1:c.591G>A XP_016856809.1:p.Lys197=
NM_005373.3:c.420G>A MANE Select NP_005364.1:p.Lys140=