Canonical Allele Identifier: CA2261354276

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351689A= , CM000679.2:g.44351689A=	GRCh38
NC_000017.10:g.42429057A= , CM000679.1:g.42429057A=	GRCh37
NC_000017.9:g.39784583A=	NCBI36
NG_007886.1:g.11567A= , LRG_661:g.11567A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1073A= MANE Select	ENSP00000053867.2:p.Gln358=
ENST00000639447.1:c.1073A=	ENSP00000492014.1:p.Gln358=
ENST00000053867.7:c.1073A=	ENSP00000053867.2:p.Gln358=
ENST00000586443.1:c.514A=
ENST00000589265.5:c.602A=	ENSP00000467616.1:p.Gln201=
ENST00000589923.1:n.331A=
NM_002087.3:c.1073A=	NP_002078.1:p.Gln358=
XM_005257253.1:c.1073A=	XP_005257310.1:p.Gln358=
XM_024450730.1:c.1073A=	XP_024306498.1:p.Gln358=
NM_002087.4:c.1073A= MANE Select	NP_002078.1:p.Gln358=