Canonical Allele Identifier: CA339974309
Community Standard Title: NM_005373.3(MPL):c.407C>G (p.Pro136Arg)
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43339286C>G , CM000663.2:g.43339286C>G GRCh38
NC_000001.10:g.43804957C>G , CM000663.1:g.43804957C>G GRCh37
NC_000001.9:g.43577544C>G NCBI36
NG_007525.1:g.6483C>G , LRG_510:g.6483C>G

Transcript Alleles

HGVS Amino-acid Change
NM_005373.3:c.407C>G MANE Select NP_005364.1:p.Pro136Arg
ENST00000372470.9:c.407C>G MANE Select ENSP00000361548.3:p.Pro136Arg
NM_005373.2:c.407C>G , LRG_510t1:c.407C>G NP_005364.1:p.Pro136Arg
ENST00000372470.7:c.407C>G ENSP00000361548.3:p.Pro136Arg
ENST00000413998.6:c.407C>G ENSP00000414004.2:p.Pro136Arg
ENST00000413998.7:c.386C>G ENSP00000414004.3:p.Pro129Arg
ENST00000612993.1:c.407C>G ENSP00000480273.1:p.Pro136Arg
ENST00000638732.1:n.407C>G
XM_011541478.1:c.386C>G XP_011539780.1:p.Pro129Arg
XM_017001320.1:c.578C>G XP_016856809.1:p.Pro193Arg