Canonical Allele Identifier: CA2809588864

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351881_44351882insT , CM000679.2:g.44351881_44351882insT	GRCh38
NC_000017.10:g.42429249_42429250insT , CM000679.1:g.42429249_42429250insT	GRCh37
NC_000017.9:g.39784775_39784776insT	NCBI36
NG_007886.1:g.11759_11760insT , LRG_661:g.11759_11760insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+86_1179+87insT MANE Select	ENSP00000053867.2:n.1179+86_1179+87insT
ENST00000639447.1:c.1136+129_1136+130insT	ENSP00000492014.1:n.1136+129_1136+130insT
ENST00000053867.7:c.1179+86_1179+87insT	ENSP00000053867.2:n.1179+86_1179+87insT
ENST00000586443.1:c.620+86_620+87insT
ENST00000589265.5:c.708+86_708+87insT	ENSP00000467616.1:n.708+86_708+87insT
NM_002087.3:c.1179+86_1179+87insT	NP_002078.1:n.1179+86_1179+87insT
XM_005257253.1:c.1179+86_1179+87insT	XP_005257310.1:n.1179+86_1179+87insT
XM_024450730.1:c.1179+86_1179+87insT	XP_024306498.1:n.1179+86_1179+87insT
NM_002087.4:c.1179+86_1179+87insT MANE Select	NP_002078.1:n.1179+86_1179+87insT