Canonical Allele Identifier: CA339987415
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1480182546

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349271T>G , CM000663.2:g.43349271T>G GRCh38
NC_000001.10:g.43814942T>G , CM000663.1:g.43814942T>G GRCh37
NC_000001.9:g.43587529T>G NCBI36
NG_007525.1:g.16468T>G , LRG_510:g.16468T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372470.9:c.1477T>G MANE Select ENSP00000361548.3:p.Ser493Ala
ENST00000413998.7:c.1456T>G ENSP00000414004.3:p.Ser486Ala
ENST00000638732.1:n.1477T>G
ENST00000643351.1:c.9T>G
ENST00000372470.7:c.1477T>G ENSP00000361548.3:p.Ser493Ala
ENST00000413998.6:c.1477T>G ENSP00000414004.2:p.Ser493Ala
ENST00000612993.1:c.1477T>G ENSP00000480273.1:p.Ser493Ala
NM_005373.2:c.1477T>G , LRG_510t1:c.1477T>G NP_005364.1:p.Ser493Ala
XM_011541478.1:c.1456T>G XP_011539780.1:p.Ser486Ala
XM_017001320.1:c.1648T>G XP_016856809.1:p.Ser550Ala
NM_005373.3:c.1477T>G MANE Select NP_005364.1:p.Ser493Ala