Canonical Allele Identifier: CA393770482
Gene: MESP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776841T>G , CM000677.2:g.89776841T>G GRCh38
NC_000015.9:g.90320072T>G , CM000677.1:g.90320072T>G GRCh37
NC_000015.8:g.88121076T>G NCBI36
NG_008608.1:g.5484T>G
NG_008608.2:g.21251T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000341735.5:c.484T>G MANE Select ENSP00000342392.3:p.Cys162Gly
ENST00000341735.3:c.484T>G ENSP00000342392.3:p.Cys162Gly
ENST00000558723.1:n.39-1224T>G
ENST00000560219.2:c.31-1224T>G ENSP00000452998.1:n.31-1224T>G
NM_001039958.1:c.484T>G NP_001035047.1:p.Cys162Gly
NM_001039958.2:c.484T>G MANE Select NP_001035047.1:p.Cys162Gly