Canonical Allele Identifier: CA1141580748
Community Standard Title: NM_005373.3(MPL):c.769C= (p.Arg257=)
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43340042C= , CM000663.2:g.43340042C= GRCh38
NC_000001.10:g.43805713C= , CM000663.1:g.43805713C= GRCh37
NC_000001.9:g.43578300C= NCBI36
NG_007525.1:g.7239C= , LRG_510:g.7239C=

Transcript Alleles

HGVS Amino-acid Change
NM_005373.3:c.769C= MANE Select NP_005364.1:p.Arg257=
ENST00000372470.9:c.769C= MANE Select ENSP00000361548.3:p.Arg257=
NM_005373.2:c.769C= , LRG_510t1:c.769C= NP_005364.1:p.Arg257=
ENST00000372470.7:c.769C= ENSP00000361548.3:p.Arg257=
ENST00000413998.6:c.769C= ENSP00000414004.2:p.Arg257=
ENST00000413998.7:c.748C= ENSP00000414004.3:p.Arg250=
ENST00000612993.1:c.769C= ENSP00000480273.1:p.Arg257=
ENST00000638732.1:n.769C=
XM_011541478.1:c.748C= XP_011539780.1:p.Arg250=
XM_017001320.1:c.940C= XP_016856809.1:p.Arg314=