Canonical Allele Identifier: CA339987652
Gene: MPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349299T>C , CM000663.2:g.43349299T>C GRCh38
NC_000001.10:g.43814970T>C , CM000663.1:g.43814970T>C GRCh37
NC_000001.9:g.43587557T>C NCBI36
NG_007525.1:g.16496T>C , LRG_510:g.16496T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1505T>C MANE Select ENSP00000361548.3:p.Leu502Pro
ENST00000413998.7:c.1484T>C ENSP00000414004.3:p.Leu495Pro
ENST00000638732.1:n.1505T>C
ENST00000643351.1:c.37T>C
ENST00000372470.7:c.1505T>C ENSP00000361548.3:p.Leu502Pro
ENST00000413998.6:c.1505T>C ENSP00000414004.2:p.Leu502Pro
ENST00000612993.1:c.1505T>C ENSP00000480273.1:p.Leu502Pro
NM_005373.2:c.1505T>C , LRG_510t1:c.1505T>C NP_005364.1:p.Leu502Pro
XM_011541478.1:c.1484T>C XP_011539780.1:p.Leu495Pro
XM_017001320.1:c.1676T>C XP_016856809.1:p.Leu559Pro
NM_005373.3:c.1505T>C MANE Select NP_005364.1:p.Leu502Pro