Canonical Allele Identifier: CA2809588868

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351889_44351890insACA , CM000679.2:g.44351889_44351890insACA	GRCh38
NC_000017.10:g.42429257_42429258insACA , CM000679.1:g.42429257_42429258insACA	GRCh37
NC_000017.9:g.39784783_39784784insACA	NCBI36
NG_007886.1:g.11767_11768insACA , LRG_661:g.11767_11768insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+94_1179+95insACA MANE Select	ENSP00000053867.2:n.1179+94_1179+95insACA
ENST00000639447.1:c.1136+137_1136+138insACA	ENSP00000492014.1:n.1136+137_1136+138insACA
ENST00000053867.7:c.1179+94_1179+95insACA	ENSP00000053867.2:n.1179+94_1179+95insACA
ENST00000586443.1:c.620+94_620+95insACA
ENST00000589265.5:c.708+94_708+95insACA	ENSP00000467616.1:n.708+94_708+95insACA
NM_002087.3:c.1179+94_1179+95insACA	NP_002078.1:n.1179+94_1179+95insACA
XM_005257253.1:c.1179+94_1179+95insACA	XP_005257310.1:n.1179+94_1179+95insACA
XM_024450730.1:c.1179+94_1179+95insACA	XP_024306498.1:n.1179+94_1179+95insACA
NM_002087.4:c.1179+94_1179+95insACA MANE Select	NP_002078.1:n.1179+94_1179+95insACA