Canonical Allele Identifier: CA2194780883
Gene: MESP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776755G= , CM000677.2:g.89776755G= GRCh38
NC_000015.9:g.90319986G= , CM000677.1:g.90319986G= GRCh37
NC_000015.8:g.88120990G= NCBI36
NG_008608.1:g.5398G=
NG_008608.2:g.21165G=

Transcript Alleles

HGVS Amino-acid change
ENST00000341735.5:c.398G= MANE Select ENSP00000342392.3:p.Gly133=
ENST00000341735.3:c.398G= ENSP00000342392.3:p.Gly133=
ENST00000558723.1:n.39-1310G=
ENST00000560219.2:c.31-1310G= ENSP00000452998.1:n.31-1310G=
NM_001039958.1:c.398G= NP_001035047.1:p.Gly133=
NM_001039958.2:c.398G= MANE Select NP_001035047.1:p.Gly133=