Canonical Allele Identifier: CA393770565
Gene: MESP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776857A>G , CM000677.2:g.89776857A>G GRCh38
NC_000015.9:g.90320088A>G , CM000677.1:g.90320088A>G GRCh37
NC_000015.8:g.88121092A>G NCBI36
NG_008608.1:g.5500A>G
NG_008608.2:g.21267A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000341735.5:c.500A>G MANE Select ENSP00000342392.3:p.Asp167Gly
ENST00000341735.3:c.500A>G ENSP00000342392.3:p.Asp167Gly
ENST00000558723.1:n.39-1208A>G
ENST00000560219.2:c.31-1208A>G ENSP00000452998.1:n.31-1208A>G
NM_001039958.1:c.500A>G NP_001035047.1:p.Asp167Gly
NM_001039958.2:c.500A>G MANE Select NP_001035047.1:p.Asp167Gly