Canonical Allele Identifier: CA393770692

Gene: MESP2

Linked Data

• MyVariant Identifiers: chr15:g.90320103A>T (hg19) ; chr15:g.89776872A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89776872A>T , CM000677.2:g.89776872A>T	GRCh38
NC_000015.9:g.90320103A>T , CM000677.1:g.90320103A>T	GRCh37
NC_000015.8:g.88121107A>T	NCBI36
NG_008608.1:g.5515A>T
NG_008608.2:g.21282A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341735.5:c.515A>T MANE Select	ENSP00000342392.3:p.Glu172Val
ENST00000341735.3:c.515A>T	ENSP00000342392.3:p.Glu172Val
ENST00000558723.1:n.39-1193A>T
ENST00000560219.2:c.31-1193A>T	ENSP00000452998.1:n.31-1193A>T
NM_001039958.1:c.515A>T	NP_001035047.1:p.Glu172Val
NM_001039958.2:c.515A>T MANE Select	NP_001035047.1:p.Glu172Val