Canonical Allele Identifier: CA339976699
Community Standard Title: NM_005373.3(MPL):c.761T>C (p.Leu254Pro)
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43340034T>C , CM000663.2:g.43340034T>C GRCh38
NC_000001.10:g.43805705T>C , CM000663.1:g.43805705T>C GRCh37
NC_000001.9:g.43578292T>C NCBI36
NG_007525.1:g.7231T>C , LRG_510:g.7231T>C

Transcript Alleles

HGVS Amino-acid Change
NM_005373.3:c.761T>C MANE Select NP_005364.1:p.Leu254Pro
ENST00000372470.9:c.761T>C MANE Select ENSP00000361548.3:p.Leu254Pro
NM_005373.2:c.761T>C , LRG_510t1:c.761T>C NP_005364.1:p.Leu254Pro
ENST00000372470.7:c.761T>C ENSP00000361548.3:p.Leu254Pro
ENST00000413998.6:c.761T>C ENSP00000414004.2:p.Leu254Pro
ENST00000413998.7:c.740T>C ENSP00000414004.3:p.Leu247Pro
ENST00000612993.1:c.761T>C ENSP00000480273.1:p.Leu254Pro
ENST00000638732.1:n.761T>C
XM_011541478.1:c.740T>C XP_011539780.1:p.Leu247Pro
XM_017001320.1:c.932T>C XP_016856809.1:p.Leu311Pro