Canonical Allele Identifier: CA772282531

Gene: GRN

Linked Data

• dbSNP Id: rs115172611
• gnomAD v3: 17-44350176-G-A
• gnomAD v4: 17-44350176-G-A
• MyVariant Identifiers: chr17:g.42427544G>A (hg19) ; chr17:g.44350176G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44350176G>A , CM000679.2:g.44350176G>A	GRCh38
NC_000017.10:g.42427544G>A , CM000679.1:g.42427544G>A	GRCh37
NC_000017.9:g.39783070G>A	NCBI36
NG_007886.1:g.10054G>A , LRG_661:g.10054G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.350-52G>A MANE Select	ENSP00000053867.2:n.350-52G>A
ENST00000639447.1:c.350-52G>A	ENSP00000492014.1:n.350-52G>A
ENST00000053867.7:c.350-52G>A	ENSP00000053867.2:n.350-52G>A
ENST00000586782.5:c.350-52G>A	ENSP00000468318.1:n.350-52G>A
ENST00000587387.5:c.392-52G>A	ENSP00000467431.1:n.392-52G>A
ENST00000587518.5:c.350-52G>A	ENSP00000465518.1:n.350-52G>A
ENST00000588143.5:c.350-52G>A	ENSP00000465375.1:n.350-52G>A
ENST00000588237.5:c.265-266G>A	ENSP00000466611.1:n.265-266G>A
ENST00000589265.5:c.350-52G>A	ENSP00000467616.1:n.350-52G>A
ENST00000591740.5:c.350-52G>A	ENSP00000467022.1:n.350-52G>A
ENST00000592783.5:c.350-52G>A	ENSP00000467870.1:n.350-52G>A
ENST00000593167.5:c.350-52G>A	ENSP00000466405.1:n.350-52G>A
NM_002087.3:c.350-52G>A	NP_002078.1:n.350-52G>A
XM_005257253.1:c.350-52G>A	XP_005257310.1:n.350-52G>A
XM_024450730.1:c.350-52G>A	XP_024306498.1:n.350-52G>A
NM_002087.4:c.350-52G>A MANE Select	NP_002078.1:n.350-52G>A