Canonical Allele Identifier: CA2695226233

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351776dup , CM000679.2:g.44351776dup	GRCh38
NC_000017.10:g.42429144dup , CM000679.1:g.42429144dup	GRCh37
NC_000017.9:g.39784670dup	NCBI36
NG_007886.1:g.11654dup , LRG_661:g.11654dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1160dup MANE Select	ENSP00000053867.2:p.Cys388LeufsTer26
ENST00000639447.1:c.1136+24dup	ENSP00000492014.1:n.1136+24dup
ENST00000053867.7:c.1160dup	ENSP00000053867.2:p.Cys388LeufsTer26
ENST00000586443.1:c.601dup
ENST00000589265.5:c.689dup	ENSP00000467616.1:p.Cys231LeufsTer26
ENST00000589923.1:n.418dup
NM_002087.3:c.1160dup	NP_002078.1:p.Cys388LeufsTer26
XM_005257253.1:c.1160dup	XP_005257310.1:p.Cys388LeufsTer26
XM_024450730.1:c.1160dup	XP_024306498.1:p.Cys388LeufsTer26
NM_002087.4:c.1160dup MANE Select	NP_002078.1:p.Cys388LeufsTer26