Canonical Allele Identifier: CA2645226425
Gene: MPL HGNC NCBI

Linked Data

gnomAD v4: 1-43349167-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43349167A>T , CM000663.2:g.43349167A>T GRCh38
NC_000001.10:g.43814838A>T , CM000663.1:g.43814838A>T GRCh37
NC_000001.9:g.43587425A>T NCBI36
NG_007525.1:g.16364A>T , LRG_510:g.16364A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.1469-96A>T MANE Select ENSP00000361548.3:n.1469-96A>T
ENST00000413998.7:c.1448-96A>T ENSP00000414004.3:n.1448-96A>T
ENST00000638732.1:n.1469-96A>T
ENST00000372470.7:c.1469-96A>T ENSP00000361548.3:n.1469-96A>T
ENST00000413998.6:c.1469-96A>T ENSP00000414004.2:n.1469-96A>T
ENST00000612993.1:c.1469-96A>T ENSP00000480273.1:n.1469-96A>T
NM_005373.2:c.1469-96A>T , LRG_510t1:c.1469-96A>T NP_005364.1:n.1469-96A>T
XM_011541478.1:c.1448-96A>T XP_011539780.1:n.1448-96A>T
XM_017001320.1:c.1640-96A>T XP_016856809.1:n.1640-96A>T
NM_005373.3:c.1469-96A>T MANE Select NP_005364.1:n.1469-96A>T