Canonical Allele Identifier: CA225199

Gene: GRN

Linked Data

• ClinVar Variation Id: 16013
• ClinVar RCV Id: RCV000017386 ; RCV000084421 ; RCV001851887
• dbSNP Id: rs63751243
• MyVariant Identifiers: chr17:g.42426558C>A (hg19) ; chr17:g.44349190C>A (hg38)
• PubMed: PMID:9633693 ; PMID:16983685 ; PMID:17984093 ; PMID:18183624 ; PMID:21482928

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44349190C>A , CM000679.2:g.44349190C>A	GRCh38
NC_000017.10:g.42426558C>A , CM000679.1:g.42426558C>A	GRCh37
NC_000017.9:g.39782084C>A	NCBI36
NG_007886.1:g.9068C>A , LRG_661:g.9068C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.26C>A MANE Select	ENSP00000053867.2:p.Ala9Asp
ENST00000639447.1:c.26C>A	ENSP00000492014.1:p.Ala9Asp
ENST00000053867.7:c.26C>A	ENSP00000053867.2:p.Ala9Asp
ENST00000585512.5:c.26C>A	ENSP00000467745.1:p.Ala9Asp
ENST00000586782.5:c.26C>A	ENSP00000468318.1:p.Ala9Asp
ENST00000587109.5:c.26C>A	ENSP00000466271.1:p.Ala9Asp
ENST00000587387.5:c.26C>A	ENSP00000467431.1:p.Ala9Asp
ENST00000587518.5:c.26C>A	ENSP00000465518.1:p.Ala9Asp
ENST00000587958.1:n.62C>A
ENST00000588143.5:c.26C>A	ENSP00000465375.1:p.Ala9Asp
ENST00000588170.5:n.122C>A
ENST00000588237.5:c.26C>A	ENSP00000466611.1:p.Ala9Asp
ENST00000589265.5:c.26C>A	ENSP00000467616.1:p.Ala9Asp
ENST00000589536.5:c.26C>A	ENSP00000466956.1:p.Ala9Asp
ENST00000591740.5:c.26C>A	ENSP00000467022.1:p.Ala9Asp
ENST00000592323.5:n.66C>A
ENST00000592783.5:c.26C>A	ENSP00000467870.1:p.Ala9Asp
ENST00000593167.5:c.26C>A	ENSP00000466405.1:p.Ala9Asp
NM_002087.3:c.26C>A	NP_002078.1:p.Ala9Asp
XM_005257253.1:c.26C>A	XP_005257310.1:p.Ala9Asp
XM_024450730.1:c.26C>A	XP_024306498.1:p.Ala9Asp
NM_002087.4:c.26C>A MANE Select	NP_002078.1:p.Ala9Asp