Canonical Allele Identifier: CA2261354503

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352110A= , CM000679.2:g.44352110A=	GRCh38
NC_000017.10:g.42429478A= , CM000679.1:g.42429478A=	GRCh37
NC_000017.9:g.39785004A=	NCBI36
NG_007886.1:g.11988A= , LRG_661:g.11988A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1275A= MANE Select	ENSP00000053867.2:p.Gly425=
ENST00000639447.1:c.1136+358A=	ENSP00000492014.1:n.1136+358A=
ENST00000053867.7:c.1275A=	ENSP00000053867.2:p.Gly425=
ENST00000586443.1:c.716A=
ENST00000589265.5:c.804A=	ENSP00000467616.1:p.Gly268=
NM_002087.3:c.1275A=	NP_002078.1:p.Gly425=
XM_005257253.1:c.1275A=	XP_005257310.1:p.Gly425=
XM_024450730.1:c.1275A=	XP_024306498.1:p.Gly425=
NM_002087.4:c.1275A= MANE Select	NP_002078.1:p.Gly425=