Canonical Allele Identifier: CA1141580747
Community Standard Title: NM_005373.3(MPL):c.556C= (p.Gln186=)
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43339435C= , CM000663.2:g.43339435C= GRCh38
NC_000001.10:g.43805106C= , CM000663.1:g.43805106C= GRCh37
NC_000001.9:g.43577693C= NCBI36
NG_007525.1:g.6632C= , LRG_510:g.6632C=

Transcript Alleles

HGVS Amino-acid Change
NM_005373.3:c.556C= MANE Select NP_005364.1:p.Gln186=
ENST00000372470.9:c.556C= MANE Select ENSP00000361548.3:p.Gln186=
NM_005373.2:c.556C= , LRG_510t1:c.556C= NP_005364.1:p.Gln186=
ENST00000372470.7:c.556C= ENSP00000361548.3:p.Gln186=
ENST00000413998.6:c.556C= ENSP00000414004.2:p.Gln186=
ENST00000413998.7:c.535C= ENSP00000414004.3:p.Gln179=
ENST00000612993.1:c.556C= ENSP00000480273.1:p.Gln186=
ENST00000638732.1:n.556C=
XM_011541478.1:c.535C= XP_011539780.1:p.Gln179=
XM_017001320.1:c.727C= XP_016856809.1:p.Gln243=