Canonical Allele Identifier: CA1165579422
Community Standard Title: NM_005373.3(MPL):c.1468+2T=
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349004T= , CM000663.2:g.43349004T= GRCh38
NC_000001.10:g.43814675T= , CM000663.1:g.43814675T= GRCh37
NC_000001.9:g.43587262T= NCBI36
NG_007525.1:g.16201T= , LRG_510:g.16201T=

Transcript Alleles

HGVS Amino-acid Change
NM_005373.3:c.1468+2T= MANE Select NP_005364.1:n.1468+2T=
ENST00000372470.9:c.1468+2T= MANE Select ENSP00000361548.3:n.1468+2T=
NM_005373.2:c.1468+2T= , LRG_510t1:c.1468+2T= NP_005364.1:n.1468+2T=
ENST00000372470.7:c.1468+2T= ENSP00000361548.3:n.1468+2T=
ENST00000413998.6:c.1468+2T= ENSP00000414004.2:n.1468+2T=
ENST00000413998.7:c.1447+2T= ENSP00000414004.3:n.1447+2T=
ENST00000612993.1:c.1468+2T= ENSP00000480273.1:n.1468+2T=
ENST00000638732.1:n.1468+2T=
XM_011541478.1:c.1447+2T= XP_011539780.1:n.1447+2T=
XM_017001320.1:c.1639+2T= XP_016856809.1:n.1639+2T=