Canonical Allele Identifier: CA2695811946
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs2153916199

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338075G>T , CM000663.2:g.43338075G>T GRCh38
NC_000001.10:g.43803746G>T , CM000663.1:g.43803746G>T GRCh37
NC_000001.9:g.43576333G>T NCBI36
NG_007525.1:g.5272G>T , LRG_510:g.5272G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.80-24G>T MANE Select ENSP00000361548.3:n.80-24G>T
ENST00000413998.7:c.80-45G>T ENSP00000414004.3:n.80-45G>T
ENST00000638732.1:n.80-24G>T
ENST00000372470.7:c.80-24G>T ENSP00000361548.3:n.80-24G>T
ENST00000413998.6:c.80-24G>T ENSP00000414004.2:n.80-24G>T
ENST00000612993.1:c.80-24G>T ENSP00000480273.1:n.80-24G>T
NM_005373.2:c.80-24G>T , LRG_510t1:c.80-24G>T NP_005364.1:n.80-24G>T
XM_011541478.1:c.80-45G>T XP_011539780.1:n.80-45G>T
XM_017001320.1:c.227G>T XP_016856809.1:p.Gly76Val
NM_005373.3:c.80-24G>T MANE Select NP_005364.1:n.80-24G>T