Canonical Allele Identifier: CA393770577
Gene: MESP2 HGNC NCBI

Linked Data

gnomAD v4: 15-89776859-C-A
MyVariant Identifiers: chr15:g.90320090C>A (hg19) chr15:g.89776859C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776859C>A , CM000677.2:g.89776859C>A GRCh38
NC_000015.9:g.90320090C>A , CM000677.1:g.90320090C>A GRCh37
NC_000015.8:g.88121094C>A NCBI36
NG_008608.1:g.5502C>A
NG_008608.2:g.21269C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341735.5:c.502C>A MANE Select ENSP00000342392.3:p.Arg168Ser
ENST00000341735.3:c.502C>A ENSP00000342392.3:p.Arg168Ser
ENST00000558723.1:n.39-1206C>A
ENST00000560219.2:c.31-1206C>A ENSP00000452998.1:n.31-1206C>A
NM_001039958.1:c.502C>A NP_001035047.1:p.Arg168Ser
NM_001039958.2:c.502C>A MANE Select NP_001035047.1:p.Arg168Ser
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