Canonical Allele Identifier: CA2194780882
Gene: MESP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776754G= , CM000677.2:g.89776754G= GRCh38
NC_000015.9:g.90319985G= , CM000677.1:g.90319985G= GRCh37
NC_000015.8:g.88120989G= NCBI36
NG_008608.1:g.5397G=
NG_008608.2:g.21164G=

Transcript Alleles

HGVS Amino-acid change
ENST00000341735.5:c.397G= MANE Select ENSP00000342392.3:p.Gly133=
ENST00000341735.3:c.397G= ENSP00000342392.3:p.Gly133=
ENST00000558723.1:n.39-1311G=
ENST00000560219.2:c.31-1311G= ENSP00000452998.1:n.31-1311G=
NM_001039958.1:c.397G= NP_001035047.1:p.Gly133=
NM_001039958.2:c.397G= MANE Select NP_001035047.1:p.Gly133=