Canonical Allele Identifier: CA399768313

Gene: GRN

Linked Data

• ClinVar Variation Id: 1455419
• ClinVar RCV Id: RCV001970022
• dbSNP Id: rs2143344360
• MyVariant Identifiers: chr17:g.42429419C>T (hg19) ; chr17:g.44352051C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352051C>T , CM000679.2:g.44352051C>T	GRCh38
NC_000017.10:g.42429419C>T , CM000679.1:g.42429419C>T	GRCh37
NC_000017.9:g.39784945C>T	NCBI36
NG_007886.1:g.11929C>T , LRG_661:g.11929C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1216C>T MANE Select	ENSP00000053867.2:p.Gln406Ter
ENST00000639447.1:c.1136+299C>T	ENSP00000492014.1:n.1136+299C>T
ENST00000053867.7:c.1216C>T	ENSP00000053867.2:p.Gln406Ter
ENST00000586443.1:c.657C>T
ENST00000589265.5:c.745C>T	ENSP00000467616.1:p.Gln249Ter
NM_002087.3:c.1216C>T	NP_002078.1:p.Gln406Ter
XM_005257253.1:c.1216C>T	XP_005257310.1:p.Gln406Ter
XM_024450730.1:c.1216C>T	XP_024306498.1:p.Gln406Ter
NM_002087.4:c.1216C>T MANE Select	NP_002078.1:p.Gln406Ter