Canonical Allele Identifier: CA2743377642
Gene: MPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43338056A>T , CM000663.2:g.43338056A>T GRCh38
NC_000001.10:g.43803727A>T , CM000663.1:g.43803727A>T GRCh37
NC_000001.9:g.43576314A>T NCBI36
NG_007525.1:g.5253A>T , LRG_510:g.5253A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372470.9:c.80-43A>T MANE Select ENSP00000361548.3:n.80-43A>T
ENST00000413998.7:c.80-64A>T ENSP00000414004.3:n.80-64A>T
ENST00000638732.1:n.80-43A>T
ENST00000372470.7:c.80-43A>T ENSP00000361548.3:n.80-43A>T
ENST00000413998.6:c.80-43A>T ENSP00000414004.2:n.80-43A>T
ENST00000612993.1:c.80-43A>T ENSP00000480273.1:n.80-43A>T
NM_005373.2:c.80-43A>T , LRG_510t1:c.80-43A>T NP_005364.1:n.80-43A>T
XM_011541478.1:c.80-64A>T XP_011539780.1:n.80-64A>T
XM_017001320.1:c.208A>T XP_016856809.1:p.Met70Leu
NM_005373.3:c.80-43A>T MANE Select NP_005364.1:n.80-43A>T