Canonical Allele Identifier: CA393769637
Gene: MESP2 HGNC NCBI

Linked Data

dbSNP Id: rs774916475
gnomAD v3: 15-89776674-G-C
gnomAD v4: 15-89776674-G-C
MyVariant Identifiers: chr15:g.90319905G>C (hg19) chr15:g.89776674G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776674G>C , CM000677.2:g.89776674G>C GRCh38
NC_000015.9:g.90319905G>C , CM000677.1:g.90319905G>C GRCh37
NC_000015.8:g.88120909G>C NCBI36
NG_008608.1:g.5317G>C
NG_008608.2:g.21084G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000341735.5:c.317G>C MANE Select ENSP00000342392.3:p.Arg106Pro
ENST00000341735.3:c.317G>C ENSP00000342392.3:p.Arg106Pro
ENST00000558723.1:n.39-1391G>C
ENST00000560219.2:c.31-1391G>C ENSP00000452998.1:n.31-1391G>C
NM_001039958.1:c.317G>C NP_001035047.1:p.Arg106Pro
NM_001039958.2:c.317G>C MANE Select NP_001035047.1:p.Arg106Pro
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