Canonical Allele Identifier: CA225346

Gene: GRN

Linked Data

• ClinVar Variation Id: 98184
• ClinVar RCV Id: RCV000084487 ; RCV000989929
• dbSNP Id: rs63749908
• gnomAD v4: 17-44352237-C-T
• MyVariant Identifiers: chr17:g.42429605C>T (hg19) ; chr17:g.44352237C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352237C>T , CM000679.2:g.44352237C>T	GRCh38
NC_000017.10:g.42429605C>T , CM000679.1:g.42429605C>T	GRCh37
NC_000017.9:g.39785131C>T	NCBI36
NG_007886.1:g.12115C>T , LRG_661:g.12115C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1402C>T MANE Select	ENSP00000053867.2:p.Gln468Ter
ENST00000639447.1:c.1137-292C>T	ENSP00000492014.1:n.1137-292C>T
ENST00000053867.7:c.1402C>T	ENSP00000053867.2:p.Gln468Ter
ENST00000586242.1:c.36C>T
ENST00000586443.1:c.843C>T
ENST00000589265.5:c.931C>T	ENSP00000467616.1:p.Gln311Ter
NM_002087.3:c.1402C>T	NP_002078.1:p.Gln468Ter
XM_005257253.1:c.1402C>T	XP_005257310.1:p.Gln468Ter
XM_024450730.1:c.1402C>T	XP_024306498.1:p.Gln468Ter
NM_002087.4:c.1402C>T MANE Select	NP_002078.1:p.Gln468Ter