Canonical Allele Identifier: CA2695226231

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351734_44351735delinsG , CM000679.2:g.44351734_44351735delinsG	GRCh38
NC_000017.10:g.42429102_42429103delinsG , CM000679.1:g.42429102_42429103delinsG	GRCh37
NC_000017.9:g.39784628_39784629delinsG	NCBI36
NG_007886.1:g.11612_11613delinsG , LRG_661:g.11612_11613delinsG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1118_1119delinsG MANE Select	ENSP00000053867.2:p.Pro373ArgfsTer?
ENST00000639447.1:c.1118_1119delinsG	ENSP00000492014.1:p.Pro373ArgfsTer?
ENST00000053867.7:c.1118_1119delinsG	ENSP00000053867.2:p.Pro373ArgfsTer?
ENST00000586443.1:c.559_560delinsG
ENST00000589265.5:c.647_648delinsG	ENSP00000467616.1:p.Pro216ArgfsTer?
ENST00000589923.1:n.376_377delinsG
NM_002087.3:c.1118_1119delinsG	NP_002078.1:p.Pro373ArgfsTer?
XM_005257253.1:c.1118_1119delinsG	XP_005257310.1:p.Pro373ArgfsTer?
XM_024450730.1:c.1118_1119delinsG	XP_024306498.1:p.Pro373ArgfsTer?
NM_002087.4:c.1118_1119delinsG MANE Select	NP_002078.1:p.Pro373ArgfsTer?