Canonical Allele Identifier: CA1165579926
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349274T= , CM000663.2:g.43349274T= GRCh38
NC_000001.10:g.43814945T= , CM000663.1:g.43814945T= GRCh37
NC_000001.9:g.43587532T= NCBI36
NG_007525.1:g.16471T= , LRG_510:g.16471T=

Transcript Alleles

HGVS Amino-acid change
ENST00000372470.9:c.1480T= MANE Select ENSP00000361548.3:p.Leu494=
ENST00000413998.7:c.1459T= ENSP00000414004.3:p.Leu487=
ENST00000638732.1:n.1480T=
ENST00000643351.1:c.12T=
ENST00000372470.7:c.1480T= ENSP00000361548.3:p.Leu494=
ENST00000413998.6:c.1480T= ENSP00000414004.2:p.Leu494=
ENST00000612993.1:c.1480T= ENSP00000480273.1:p.Leu494=
NM_005373.2:c.1480T= , LRG_510t1:c.1480T= NP_005364.1:p.Leu494=
XM_011541478.1:c.1459T= XP_011539780.1:p.Leu487=
XM_017001320.1:c.1651T= XP_016856809.1:p.Leu551=
NM_005373.3:c.1480T= MANE Select NP_005364.1:p.Leu494=