Canonical Allele Identifier: CA2261354426

Gene: GRN

Linked Data

• dbSNP Id: rs2048379534
• gnomAD v3: 17-44351967-G-A
• gnomAD v4: 17-44351967-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351967G>A , CM000679.2:g.44351967G>A	GRCh38
NC_000017.10:g.42429335G>A , CM000679.1:g.42429335G>A	GRCh37
NC_000017.9:g.39784861G>A	NCBI36
NG_007886.1:g.11845G>A , LRG_661:g.11845G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1180-48G>A MANE Select	ENSP00000053867.2:n.1180-48G>A
ENST00000639447.1:c.1136+215G>A	ENSP00000492014.1:n.1136+215G>A
ENST00000053867.7:c.1180-48G>A	ENSP00000053867.2:n.1180-48G>A
ENST00000586443.1:c.621-48G>A
ENST00000589265.5:c.709-48G>A	ENSP00000467616.1:n.709-48G>A
NM_002087.3:c.1180-48G>A	NP_002078.1:n.1180-48G>A
XM_005257253.1:c.1180-48G>A	XP_005257310.1:n.1180-48G>A
XM_024450730.1:c.1180-48G>A	XP_024306498.1:n.1180-48G>A
NM_002087.4:c.1180-48G>A MANE Select	NP_002078.1:n.1180-48G>A