Canonical Allele Identifier: CA2187545229

Gene: ISLR2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74132860G= , CM000677.2:g.74132860G=	GRCh38
NC_000015.9:g.74425201G= , CM000677.1:g.74425201G=	GRCh37
NC_000015.8:g.72212254G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020851.3:c.106G= MANE Select	NP_065902.1:p.Asp36=
ENST00000453268.3:c.106G= MANE Select	ENSP00000411834.2:p.Asp36=
NM_001130136.1:c.106G=	NP_001123608.1:p.Asp36=
NM_001130137.1:c.106G=	NP_001123609.1:p.Asp36=
NM_001130138.1:c.106G=	NP_001123610.1:p.Asp36=
NM_001130138.2:c.106G=	NP_001123610.1:p.Asp36=
NM_020851.2:c.106G=	NP_065902.1:p.Asp36=
ENST00000361742.7:c.106G=	ENSP00000355402.3:p.Asp36=
ENST00000419208.2:c.106G=	ENSP00000408872.2:p.Asp36=
ENST00000435464.5:c.106G=	ENSP00000411443.1:p.Asp36=
ENST00000453268.2:c.106G=	ENSP00000411834.2:p.Asp36=
ENST00000561740.5:c.106G=	ENSP00000455076.1:p.Asp36=
ENST00000561975.5:n.338+1544G=
ENST00000565159.5:c.106G=	ENSP00000455531.1:p.Asp36=
ENST00000565332.1:c.106G=	ENSP00000454259.1:p.Asp36=
ENST00000565540.1:c.106G=	ENSP00000458080.1:p.Asp36=
ENST00000569886.5:c.106G=	ENSP00000454287.1:p.Asp36=
XM_011521840.1:c.106G=	XP_011520142.1:p.Asp36=
XM_011521840.3:c.106G=	XP_011520142.1:p.Asp36=
XM_011521841.1:c.106G=	XP_011520143.1:p.Asp36=
XM_011521842.1:c.106G=	XP_011520144.1:p.Asp36=
XM_017022446.2:c.106G=	XP_016877935.1:p.Asp36=
XM_024450003.1:c.106G=	XP_024305771.1:p.Asp36=
XM_024450004.1:c.106G=	XP_024305772.1:p.Asp36=
XM_024450005.1:c.106G=	XP_024305773.1:p.Asp36=
XM_024450006.1:c.106G=	XP_024305774.1:p.Asp36=
XM_024450007.1:c.106G=	XP_024305775.1:p.Asp36=
XM_024450008.1:c.106G=	XP_024305776.1:p.Asp36=
XR_931875.1:n.224G=
XR_931875.3:n.444G=