Canonical Allele Identifier: CA2809588862

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351870_44351871insCAG , CM000679.2:g.44351870_44351871insCAG	GRCh38
NC_000017.10:g.42429238_42429239insCAG , CM000679.1:g.42429238_42429239insCAG	GRCh37
NC_000017.9:g.39784764_39784765insCAG	NCBI36
NG_007886.1:g.11748_11749insCAG , LRG_661:g.11748_11749insCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+75_1179+76insCAG MANE Select	ENSP00000053867.2:n.1179+75_1179+76insCAG
ENST00000639447.1:c.1136+118_1136+119insCAG	ENSP00000492014.1:n.1136+118_1136+119insCAG
ENST00000053867.7:c.1179+75_1179+76insCAG	ENSP00000053867.2:n.1179+75_1179+76insCAG
ENST00000586443.1:c.620+75_620+76insCAG
ENST00000589265.5:c.708+75_708+76insCAG	ENSP00000467616.1:n.708+75_708+76insCAG
NM_002087.3:c.1179+75_1179+76insCAG	NP_002078.1:n.1179+75_1179+76insCAG
XM_005257253.1:c.1179+75_1179+76insCAG	XP_005257310.1:n.1179+75_1179+76insCAG
XM_024450730.1:c.1179+75_1179+76insCAG	XP_024306498.1:n.1179+75_1179+76insCAG
NM_002087.4:c.1179+75_1179+76insCAG MANE Select	NP_002078.1:n.1179+75_1179+76insCAG