Canonical Allele Identifier: CA492295417
Gene: MESP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.90320101A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776870A>T , CM000677.2:g.89776870A>T GRCh38
NC_000015.9:g.90320101A>T , CM000677.1:g.90320101A>T GRCh37
NC_000015.8:g.88121105A>T NCBI36
NG_008608.1:g.5513A>T
NG_008608.2:g.21280A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000341735.5:c.513A>T MANE Select ENSP00000342392.3:p.Ala171=
ENST00000341735.3:c.513A>T ENSP00000342392.3:p.Ala171=
ENST00000558723.1:n.39-1195A>T
ENST00000560219.2:c.31-1195A>T ENSP00000452998.1:n.31-1195A>T
NM_001039958.1:c.513A>T NP_001035047.1:p.Ala171=
NM_001039958.2:c.513A>T MANE Select NP_001035047.1:p.Ala171=