Canonical Allele Identifier: CA393770037
Gene: MESP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776758A>C , CM000677.2:g.89776758A>C GRCh38
NC_000015.9:g.90319989A>C , CM000677.1:g.90319989A>C GRCh37
NC_000015.8:g.88120993A>C NCBI36
NG_008608.1:g.5401A>C
NG_008608.2:g.21168A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000341735.5:c.401A>C MANE Select ENSP00000342392.3:p.His134Pro
ENST00000341735.3:c.401A>C ENSP00000342392.3:p.His134Pro
ENST00000558723.1:n.39-1307A>C
ENST00000560219.2:c.31-1307A>C ENSP00000452998.1:n.31-1307A>C
NM_001039958.1:c.401A>C NP_001035047.1:p.His134Pro
NM_001039958.2:c.401A>C MANE Select NP_001035047.1:p.His134Pro