Canonical Allele Identifier: CA2261354285

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351708C= , CM000679.2:g.44351708C=	GRCh38
NC_000017.10:g.42429076C= , CM000679.1:g.42429076C=	GRCh37
NC_000017.9:g.39784602C=	NCBI36
NG_007886.1:g.11586C= , LRG_661:g.11586C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1092C= MANE Select	ENSP00000053867.2:p.Val364=
ENST00000639447.1:c.1092C=	ENSP00000492014.1:p.Val364=
ENST00000053867.7:c.1092C=	ENSP00000053867.2:p.Val364=
ENST00000586443.1:c.533C=
ENST00000589265.5:c.621C=	ENSP00000467616.1:p.Val207=
ENST00000589923.1:n.350C=
NM_002087.3:c.1092C=	NP_002078.1:p.Val364=
XM_005257253.1:c.1092C=	XP_005257310.1:p.Val364=
XM_024450730.1:c.1092C=	XP_024306498.1:p.Val364=
NM_002087.4:c.1092C= MANE Select	NP_002078.1:p.Val364=