Canonical Allele Identifier: CA626224212

Gene: GRN

Linked Data

• dbSNP Id: rs1465603049
• gnomAD v2: 17-42429341-C-T
• gnomAD v4: 17-44351973-C-T
• MyVariant Identifiers: chr17:g.42429341C>T (hg19) ; chr17:g.44351973C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351973C>T , CM000679.2:g.44351973C>T	GRCh38
NC_000017.10:g.42429341C>T , CM000679.1:g.42429341C>T	GRCh37
NC_000017.9:g.39784867C>T	NCBI36
NG_007886.1:g.11851C>T , LRG_661:g.11851C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1180-42C>T MANE Select	ENSP00000053867.2:n.1180-42C>T
ENST00000639447.1:c.1136+221C>T	ENSP00000492014.1:n.1136+221C>T
ENST00000053867.7:c.1180-42C>T	ENSP00000053867.2:n.1180-42C>T
ENST00000586443.1:c.621-42C>T
ENST00000589265.5:c.709-42C>T	ENSP00000467616.1:n.709-42C>T
NM_002087.3:c.1180-42C>T	NP_002078.1:n.1180-42C>T
XM_005257253.1:c.1180-42C>T	XP_005257310.1:n.1180-42C>T
XM_024450730.1:c.1180-42C>T	XP_024306498.1:n.1180-42C>T
NM_002087.4:c.1180-42C>T MANE Select	NP_002078.1:n.1180-42C>T