Canonical Allele Identifier: CA399765600

Gene: GRN

Linked Data

• ClinVar Variation Id: 2193378
• ClinVar RCV Id: RCV002623945
• dbSNP Id: rs1348717018
• MyVariant Identifiers: chr17:g.42429043C>G (hg19) ; chr17:g.44351675C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351675C>G , CM000679.2:g.44351675C>G	GRCh38
NC_000017.10:g.42429043C>G , CM000679.1:g.42429043C>G	GRCh37
NC_000017.9:g.39784569C>G	NCBI36
NG_007886.1:g.11553C>G , LRG_661:g.11553C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1059C>G MANE Select	ENSP00000053867.2:p.Ser353Arg
ENST00000639447.1:c.1059C>G	ENSP00000492014.1:p.Ser353Arg
ENST00000053867.7:c.1059C>G	ENSP00000053867.2:p.Ser353Arg
ENST00000586443.1:c.500C>G
ENST00000589265.5:c.588C>G	ENSP00000467616.1:p.Ser196Arg
ENST00000589923.1:n.317C>G
NM_002087.3:c.1059C>G	NP_002078.1:p.Ser353Arg
XM_005257253.1:c.1059C>G	XP_005257310.1:p.Ser353Arg
XM_024450730.1:c.1059C>G	XP_024306498.1:p.Ser353Arg
NM_002087.4:c.1059C>G MANE Select	NP_002078.1:p.Ser353Arg