Canonical Allele Identifier: CA2809588850

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351844_44351847del , CM000679.2:g.44351844_44351847del	GRCh38
NC_000017.10:g.42429212_42429215del , CM000679.1:g.42429212_42429215del	GRCh37
NC_000017.9:g.39784738_39784741del	NCBI36
NG_007886.1:g.11722_11725del , LRG_661:g.11722_11725del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+49_1179+52del MANE Select	ENSP00000053867.2:n.1179+49_1179+52del
ENST00000639447.1:c.1136+92_1136+95del	ENSP00000492014.1:n.1136+92_1136+95del
ENST00000053867.7:c.1179+49_1179+52del	ENSP00000053867.2:n.1179+49_1179+52del
ENST00000586443.1:c.620+49_620+52del
ENST00000589265.5:c.708+49_708+52del	ENSP00000467616.1:n.708+49_708+52del
NM_002087.3:c.1179+49_1179+52del	NP_002078.1:n.1179+49_1179+52del
XM_005257253.1:c.1179+49_1179+52del	XP_005257310.1:n.1179+49_1179+52del
XM_024450730.1:c.1179+49_1179+52del	XP_024306498.1:n.1179+49_1179+52del
NM_002087.4:c.1179+49_1179+52del MANE Select	NP_002078.1:n.1179+49_1179+52del