Canonical Allele Identifier: CA339973505
Gene: MPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338616C>A , CM000663.2:g.43338616C>A GRCh38
NC_000001.10:g.43804287C>A , CM000663.1:g.43804287C>A GRCh37
NC_000001.9:g.43576874C>A NCBI36
NG_007525.1:g.5813C>A , LRG_510:g.5813C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.287C>A MANE Select ENSP00000361548.3:p.Pro96Gln
ENST00000413998.7:c.266C>A ENSP00000414004.3:p.Pro89Gln
ENST00000638732.1:n.287C>A
ENST00000372470.7:c.287C>A ENSP00000361548.3:p.Pro96Gln
ENST00000413998.6:c.287C>A ENSP00000414004.2:p.Pro96Gln
ENST00000612993.1:c.287C>A ENSP00000480273.1:p.Pro96Gln
NM_005373.2:c.287C>A , LRG_510t1:c.287C>A NP_005364.1:p.Pro96Gln
XM_011541478.1:c.266C>A XP_011539780.1:p.Pro89Gln
XM_017001320.1:c.458C>A XP_016856809.1:p.Pro153Gln
NM_005373.3:c.287C>A MANE Select NP_005364.1:p.Pro96Gln