Canonical Allele Identifier: CA1165576028
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338494G= , CM000663.2:g.43338494G= GRCh38
NC_000001.10:g.43804165G= , CM000663.1:g.43804165G= GRCh37
NC_000001.9:g.43576752G= NCBI36
NG_007525.1:g.5691G= , LRG_510:g.5691G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.213-48G= MANE Select ENSP00000361548.3:n.213-48G=
ENST00000413998.7:c.192-48G= ENSP00000414004.3:n.192-48G=
ENST00000638732.1:n.213-48G=
ENST00000372470.7:c.213-48G= ENSP00000361548.3:n.213-48G=
ENST00000413998.6:c.213-48G= ENSP00000414004.2:n.213-48G=
ENST00000612993.1:c.213-48G= ENSP00000480273.1:n.213-48G=
NM_005373.2:c.213-48G= , LRG_510t1:c.213-48G= NP_005364.1:n.213-48G=
XM_011541478.1:c.192-48G= XP_011539780.1:n.192-48G=
XM_017001320.1:c.384-48G= XP_016856809.1:n.384-48G=
NM_005373.3:c.213-48G= MANE Select NP_005364.1:n.213-48G=