Canonical Allele Identifier: CA393769650
Gene: MESP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.90319908T>G (hg19) chr15:g.89776677T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000341735.5:c.320T>G MANE Select ENSP00000342392.3:p.Phe107Cys
ENST00000341735.3:c.320T>G ENSP00000342392.3:p.Phe107Cys
ENST00000558723.1:n.39-1388T>G
ENST00000560219.2:c.31-1388T>G ENSP00000452998.1:n.31-1388T>G
NM_001039958.1:c.320T>G NP_001035047.1:p.Phe107Cys
NM_001039958.2:c.320T>G MANE Select NP_001035047.1:p.Phe107Cys
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