Canonical Allele Identifier: CA2261354335

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351796_44351798delinsGTA , CM000679.2:g.44351796_44351798delinsGTA	GRCh38
NC_000017.10:g.42429164_42429166delinsGTA , CM000679.1:g.42429164_42429166delinsGTA	GRCh37
NC_000017.9:g.39784690_39784692delinsGTA	NCBI36
NG_007886.1:g.11674_11676delinsGTA , LRG_661:g.11674_11676delinsGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+1_1179+3delinsGTA MANE Select	ENSP00000053867.2:n.1179+1_1179+3delinsGTA
ENST00000639447.1:c.1136+44_1136+46delinsGTA	ENSP00000492014.1:n.1136+44_1136+46delinsGTA
ENST00000053867.7:c.1179+1_1179+3delinsGTA	ENSP00000053867.2:n.1179+1_1179+3delinsGTA
ENST00000586443.1:c.620+1_620+3delinsGTA
ENST00000589265.5:c.708+1_708+3delinsGTA	ENSP00000467616.1:n.708+1_708+3delinsGTA
NM_002087.3:c.1179+1_1179+3delinsGTA	NP_002078.1:n.1179+1_1179+3delinsGTA
XM_005257253.1:c.1179+1_1179+3delinsGTA	XP_005257310.1:n.1179+1_1179+3delinsGTA
XM_024450730.1:c.1179+1_1179+3delinsGTA	XP_024306498.1:n.1179+1_1179+3delinsGTA
NM_002087.4:c.1179+1_1179+3delinsGTA MANE Select	NP_002078.1:n.1179+1_1179+3delinsGTA