Canonical Allele Identifier: CA393770653
Gene: MESP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.90320099G>C (hg19) chr15:g.89776868G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776868G>C , CM000677.2:g.89776868G>C GRCh38
NC_000015.9:g.90320099G>C , CM000677.1:g.90320099G>C GRCh37
NC_000015.8:g.88121103G>C NCBI36
NG_008608.1:g.5511G>C
NG_008608.2:g.21278G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000341735.5:c.511G>C MANE Select ENSP00000342392.3:p.Ala171Pro
ENST00000341735.3:c.511G>C ENSP00000342392.3:p.Ala171Pro
ENST00000558723.1:n.39-1197G>C
ENST00000560219.2:c.31-1197G>C ENSP00000452998.1:n.31-1197G>C
NM_001039958.1:c.511G>C NP_001035047.1:p.Ala171Pro
NM_001039958.2:c.511G>C MANE Select NP_001035047.1:p.Ala171Pro
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