Canonical Allele Identifier: CA393769648
Gene: MESP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.90319908T>A (hg19) chr15:g.89776677T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776677T>A , CM000677.2:g.89776677T>A GRCh38
NC_000015.9:g.90319908T>A , CM000677.1:g.90319908T>A GRCh37
NC_000015.8:g.88120912T>A NCBI36
NG_008608.1:g.5320T>A
NG_008608.2:g.21087T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341735.5:c.320T>A MANE Select ENSP00000342392.3:p.Phe107Tyr
ENST00000341735.3:c.320T>A ENSP00000342392.3:p.Phe107Tyr
ENST00000558723.1:n.39-1388T>A
ENST00000560219.2:c.31-1388T>A ENSP00000452998.1:n.31-1388T>A
NM_001039958.1:c.320T>A NP_001035047.1:p.Phe107Tyr
NM_001039958.2:c.320T>A MANE Select NP_001035047.1:p.Phe107Tyr
Search 100 bp 5'
Search 100 bp 3'