Canonical Allele Identifier: CA1165579931
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349278T= , CM000663.2:g.43349278T= GRCh38
NC_000001.10:g.43814949T= , CM000663.1:g.43814949T= GRCh37
NC_000001.9:g.43587536T= NCBI36
NG_007525.1:g.16475T= , LRG_510:g.16475T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1484T= MANE Select ENSP00000361548.3:p.Val495=
ENST00000413998.7:c.1463T= ENSP00000414004.3:p.Val488=
ENST00000638732.1:n.1484T=
ENST00000643351.1:c.16T=
ENST00000372470.7:c.1484T= ENSP00000361548.3:p.Val495=
ENST00000413998.6:c.1484T= ENSP00000414004.2:p.Val495=
ENST00000612993.1:c.1484T= ENSP00000480273.1:p.Val495=
NM_005373.2:c.1484T= , LRG_510t1:c.1484T= NP_005364.1:p.Val495=
XM_011541478.1:c.1463T= XP_011539780.1:p.Val488=
XM_017001320.1:c.1655T= XP_016856809.1:p.Val552=
NM_005373.3:c.1484T= MANE Select NP_005364.1:p.Val495=