Canonical Allele Identifier: CA2809588843

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351679_44351680del , CM000679.2:g.44351679_44351680del	GRCh38
NC_000017.10:g.42429047_42429048del , CM000679.1:g.42429047_42429048del	GRCh37
NC_000017.9:g.39784573_39784574del	NCBI36
NG_007886.1:g.11557_11558del , LRG_661:g.11557_11558del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1063_1064del MANE Select	ENSP00000053867.2:p.Pro355ArgfsTer12
ENST00000639447.1:c.1063_1064del	ENSP00000492014.1:p.Pro355ArgfsTer12
ENST00000053867.7:c.1063_1064del	ENSP00000053867.2:p.Pro355ArgfsTer12
ENST00000586443.1:c.504_505del
ENST00000589265.5:c.592_593del	ENSP00000467616.1:p.Pro198ArgfsTer12
ENST00000589923.1:n.321_322del
NM_002087.3:c.1063_1064del	NP_002078.1:p.Pro355ArgfsTer12
XM_005257253.1:c.1063_1064del	XP_005257310.1:p.Pro355ArgfsTer12
XM_024450730.1:c.1063_1064del	XP_024306498.1:p.Pro355ArgfsTer12
NM_002087.4:c.1063_1064del MANE Select	NP_002078.1:p.Pro355ArgfsTer12