Canonical Allele Identifier: CA2261354245

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351622G= , CM000679.2:g.44351622G=	GRCh38
NC_000017.10:g.42428990G= , CM000679.1:g.42428990G=	GRCh37
NC_000017.9:g.39784516G=	NCBI36
NG_007886.1:g.11500G= , LRG_661:g.11500G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1006G= MANE Select	ENSP00000053867.2:p.Glu336=
ENST00000639447.1:c.1006G=	ENSP00000492014.1:p.Glu336=
ENST00000053867.7:c.1006G=	ENSP00000053867.2:p.Glu336=
ENST00000586443.1:c.447G=
ENST00000589265.5:c.535G=	ENSP00000467616.1:p.Glu179=
ENST00000589923.1:n.264G=
NM_002087.3:c.1006G=	NP_002078.1:p.Glu336=
XM_005257253.1:c.1006G=	XP_005257310.1:p.Glu336=
XM_024450730.1:c.1006G=	XP_024306498.1:p.Glu336=
NM_002087.4:c.1006G= MANE Select	NP_002078.1:p.Glu336=