Canonical Allele Identifier: CA1165576068
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338604T= , CM000663.2:g.43338604T= GRCh38
NC_000001.10:g.43804275T= , CM000663.1:g.43804275T= GRCh37
NC_000001.9:g.43576862T= NCBI36
NG_007525.1:g.5801T= , LRG_510:g.5801T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.275T= MANE Select ENSP00000361548.3:p.Val92=
ENST00000413998.7:c.254T= ENSP00000414004.3:p.Val85=
ENST00000638732.1:n.275T=
ENST00000372470.7:c.275T= ENSP00000361548.3:p.Val92=
ENST00000413998.6:c.275T= ENSP00000414004.2:p.Val92=
ENST00000612993.1:c.275T= ENSP00000480273.1:p.Val92=
NM_005373.2:c.275T= , LRG_510t1:c.275T= NP_005364.1:p.Val92=
XM_011541478.1:c.254T= XP_011539780.1:p.Val85=
XM_017001320.1:c.446T= XP_016856809.1:p.Val149=
NM_005373.3:c.275T= MANE Select NP_005364.1:p.Val92=