Canonical Allele Identifier: CA2261354615

Gene: GRN

Linked Data

• dbSNP Id: rs2048384780
• gnomAD v4: 17-44352330-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352330T>A , CM000679.2:g.44352330T>A	GRCh38
NC_000017.10:g.42429698T>A , CM000679.1:g.42429698T>A	GRCh37
NC_000017.9:g.39785224T>A	NCBI36
NG_007886.1:g.12208T>A , LRG_661:g.12208T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1414-11T>A MANE Select	ENSP00000053867.2:n.1414-11T>A
ENST00000639447.1:c.1137-199T>A	ENSP00000492014.1:n.1137-199T>A
ENST00000053867.7:c.1414-11T>A	ENSP00000053867.2:n.1414-11T>A
ENST00000586242.1:c.48-11T>A
ENST00000586443.1:c.855-11T>A
ENST00000589265.5:c.943-11T>A	ENSP00000467616.1:n.943-11T>A
NM_002087.3:c.1414-11T>A	NP_002078.1:n.1414-11T>A
XM_005257253.1:c.1414-11T>A	XP_005257310.1:n.1414-11T>A
XM_024450730.1:c.1414-11T>A	XP_024306498.1:n.1414-11T>A
NM_002087.4:c.1414-11T>A MANE Select	NP_002078.1:n.1414-11T>A