Canonical Allele Identifier: CA1165575816
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337955C= , CM000663.2:g.43337955C= GRCh38
NC_000001.10:g.43803626C= , CM000663.1:g.43803626C= GRCh37
NC_000001.9:g.43576213C= NCBI36
NG_007525.1:g.5152C= , LRG_510:g.5152C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.79+28C= MANE Select ENSP00000361548.3:n.79+28C=
ENST00000413998.7:c.79+28C= ENSP00000414004.3:n.79+28C=
ENST00000638732.1:n.79+28C=
ENST00000372470.7:c.79+28C= ENSP00000361548.3:n.79+28C=
ENST00000413998.6:c.79+28C= ENSP00000414004.2:n.79+28C=
ENST00000612993.1:c.79+28C= ENSP00000480273.1:n.79+28C=
NM_005373.2:c.79+28C= , LRG_510t1:c.79+28C= NP_005364.1:n.79+28C=
XM_011541478.1:c.79+28C= XP_011539780.1:n.79+28C=
XM_017001320.1:c.107C= XP_016856809.1:p.Pro36=
NM_005373.3:c.79+28C= MANE Select NP_005364.1:n.79+28C=