Canonical Allele Identifier: CA2695581043
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1647005058
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337938C>A , CM000663.2:g.43337938C>A GRCh38
NC_000001.10:g.43803609C>A , CM000663.1:g.43803609C>A GRCh37
NC_000001.9:g.43576196C>A NCBI36
NG_007525.1:g.5135C>A , LRG_510:g.5135C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.79+11C>A MANE Select ENSP00000361548.3:n.79+11C>A
ENST00000413998.7:c.79+11C>A ENSP00000414004.3:n.79+11C>A
ENST00000638732.1:n.79+11C>A
ENST00000372470.7:c.79+11C>A ENSP00000361548.3:n.79+11C>A
ENST00000413998.6:c.79+11C>A ENSP00000414004.2:n.79+11C>A
ENST00000612993.1:c.79+11C>A ENSP00000480273.1:n.79+11C>A
NM_005373.2:c.79+11C>A , LRG_510t1:c.79+11C>A NP_005364.1:n.79+11C>A
XM_011541478.1:c.79+11C>A XP_011539780.1:n.79+11C>A
XM_017001320.1:c.90C>A XP_016856809.1:p.His30Gln
NM_005373.3:c.79+11C>A MANE Select NP_005364.1:n.79+11C>A
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