Canonical Allele Identifier: CA2194780911

Gene: MESP2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89776809G= , CM000677.2:g.89776809G=	GRCh38
NC_000015.9:g.90320040G= , CM000677.1:g.90320040G=	GRCh37
NC_000015.8:g.88121044G=	NCBI36
NG_008608.1:g.5452G=
NG_008608.2:g.21219G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341735.5:c.452G= MANE Select	ENSP00000342392.3:p.Arg151=
ENST00000341735.3:c.452G=	ENSP00000342392.3:p.Arg151=
ENST00000558723.1:n.39-1256G=
ENST00000560219.2:c.31-1256G=	ENSP00000452998.1:n.31-1256G=
NM_001039958.1:c.452G=	NP_001035047.1:p.Arg151=
NM_001039958.2:c.452G= MANE Select	NP_001035047.1:p.Arg151=