Canonical Allele Identifier: CA2194780732

Gene: MESP2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89776540C= , CM000677.2:g.89776540C=	GRCh38
NC_000015.9:g.90319771C= , CM000677.1:g.90319771C=	GRCh37
NC_000015.8:g.88120775C=	NCBI36
NG_008608.1:g.5183C=
NG_008608.2:g.20950C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000341735.5:c.183C= MANE Select	ENSP00000342392.3:p.Ser61=
ENST00000341735.3:c.183C=	ENSP00000342392.3:p.Ser61=
ENST00000558723.1:n.39-1525C=
ENST00000560219.2:c.31-1525C=	ENSP00000452998.1:n.31-1525C=
NM_001039958.1:c.183C=	NP_001035047.1:p.Ser61=
NM_001039958.2:c.183C= MANE Select	NP_001035047.1:p.Ser61=