Canonical Allele Identifier: CA2695581048
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1647005341
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337988T>A , CM000663.2:g.43337988T>A GRCh38
NC_000001.10:g.43803659T>A , CM000663.1:g.43803659T>A GRCh37
NC_000001.9:g.43576246T>A NCBI36
NG_007525.1:g.5185T>A , LRG_510:g.5185T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.79+61T>A MANE Select ENSP00000361548.3:n.79+61T>A
ENST00000413998.7:c.79+61T>A ENSP00000414004.3:n.79+61T>A
ENST00000638732.1:n.79+61T>A
ENST00000372470.7:c.79+61T>A ENSP00000361548.3:n.79+61T>A
ENST00000413998.6:c.79+61T>A ENSP00000414004.2:n.79+61T>A
ENST00000612993.1:c.79+61T>A ENSP00000480273.1:n.79+61T>A
NM_005373.2:c.79+61T>A , LRG_510t1:c.79+61T>A NP_005364.1:n.79+61T>A
XM_011541478.1:c.79+61T>A XP_011539780.1:n.79+61T>A
XM_017001320.1:c.140T>A XP_016856809.1:p.Met47Lys
NM_005373.3:c.79+61T>A MANE Select NP_005364.1:n.79+61T>A
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