Canonical Allele Identifier: CA2638209899

Gene: GRN

Linked Data

• gnomAD v4: 17-44351772-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351776del , CM000679.2:g.44351776del	GRCh38
NC_000017.10:g.42429144del , CM000679.1:g.42429144del	GRCh37
NC_000017.9:g.39784670del	NCBI36
NG_007886.1:g.11654del , LRG_661:g.11654del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1160del MANE Select	ENSP00000053867.2:p.Gly387AlafsTer25
ENST00000639447.1:c.1136+24del	ENSP00000492014.1:n.1136+24del
ENST00000053867.7:c.1160del	ENSP00000053867.2:p.Gly387AlafsTer25
ENST00000586443.1:c.601del
ENST00000589265.5:c.689del	ENSP00000467616.1:p.Gly230AlafsTer25
ENST00000589923.1:n.418del
NM_002087.3:c.1160del	NP_002078.1:p.Gly387AlafsTer25
XM_005257253.1:c.1160del	XP_005257310.1:p.Gly387AlafsTer25
XM_024450730.1:c.1160del	XP_024306498.1:p.Gly387AlafsTer25
NM_002087.4:c.1160del MANE Select	NP_002078.1:p.Gly387AlafsTer25