Canonical Allele Identifier: CA2695811654
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs2153916194

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338068A>T , CM000663.2:g.43338068A>T GRCh38
NC_000001.10:g.43803739A>T , CM000663.1:g.43803739A>T GRCh37
NC_000001.9:g.43576326A>T NCBI36
NG_007525.1:g.5265A>T , LRG_510:g.5265A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.80-31A>T MANE Select ENSP00000361548.3:n.80-31A>T
ENST00000413998.7:c.80-52A>T ENSP00000414004.3:n.80-52A>T
ENST00000638732.1:n.80-31A>T
ENST00000372470.7:c.80-31A>T ENSP00000361548.3:n.80-31A>T
ENST00000413998.6:c.80-31A>T ENSP00000414004.2:n.80-31A>T
ENST00000612993.1:c.80-31A>T ENSP00000480273.1:n.80-31A>T
NM_005373.2:c.80-31A>T , LRG_510t1:c.80-31A>T NP_005364.1:n.80-31A>T
XM_011541478.1:c.80-52A>T XP_011539780.1:n.80-52A>T
XM_017001320.1:c.220A>T XP_016856809.1:p.Thr74Ser
NM_005373.3:c.80-31A>T MANE Select NP_005364.1:n.80-31A>T