Canonical Allele Identifier: CA2638209999

Gene: GRN

Linked Data

• gnomAD v4: 17-44351875-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351876del , CM000679.2:g.44351876del	GRCh38
NC_000017.10:g.42429244del , CM000679.1:g.42429244del	GRCh37
NC_000017.9:g.39784770del	NCBI36
NG_007886.1:g.11754del , LRG_661:g.11754del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+81del MANE Select	ENSP00000053867.2:n.1179+81del
ENST00000639447.1:c.1136+124del	ENSP00000492014.1:n.1136+124del
ENST00000053867.7:c.1179+81del	ENSP00000053867.2:n.1179+81del
ENST00000586443.1:c.620+81del
ENST00000589265.5:c.708+81del	ENSP00000467616.1:n.708+81del
NM_002087.3:c.1179+81del	NP_002078.1:n.1179+81del
XM_005257253.1:c.1179+81del	XP_005257310.1:n.1179+81del
XM_024450730.1:c.1179+81del	XP_024306498.1:n.1179+81del
NM_002087.4:c.1179+81del MANE Select	NP_002078.1:n.1179+81del