Canonical Allele Identifier: CA339987455
Gene: MPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349272C>T , CM000663.2:g.43349272C>T GRCh38
NC_000001.10:g.43814943C>T , CM000663.1:g.43814943C>T GRCh37
NC_000001.9:g.43587530C>T NCBI36
NG_007525.1:g.16469C>T , LRG_510:g.16469C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372470.9:c.1478C>T MANE Select ENSP00000361548.3:p.Ser493Phe
ENST00000413998.7:c.1457C>T ENSP00000414004.3:p.Ser486Phe
ENST00000638732.1:n.1478C>T
ENST00000643351.1:c.10C>T
ENST00000372470.7:c.1478C>T ENSP00000361548.3:p.Ser493Phe
ENST00000413998.6:c.1478C>T ENSP00000414004.2:p.Ser493Phe
ENST00000612993.1:c.1478C>T ENSP00000480273.1:p.Ser493Phe
NM_005373.2:c.1478C>T , LRG_510t1:c.1478C>T NP_005364.1:p.Ser493Phe
XM_011541478.1:c.1457C>T XP_011539780.1:p.Ser486Phe
XM_017001320.1:c.1649C>T XP_016856809.1:p.Ser550Phe
NM_005373.3:c.1478C>T MANE Select NP_005364.1:p.Ser493Phe