Canonical Allele Identifier: CA8602197

Gene: GRN

Linked Data

• dbSNP Id: rs761708338
• ExAC: 17:42429672 G / A
• gnomAD v2: 17-42429672-G-A
• gnomAD v4: 17-44352304-G-A
• MyVariant Identifiers: chr17:g.42429672G>A (hg19) ; chr17:g.44352304G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352304G>A , CM000679.2:g.44352304G>A	GRCh38
NC_000017.10:g.42429672G>A , CM000679.1:g.42429672G>A	GRCh37
NC_000017.9:g.39785198G>A	NCBI36
NG_007886.1:g.12182G>A , LRG_661:g.12182G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1414-37G>A MANE Select	ENSP00000053867.2:n.1414-37G>A
ENST00000639447.1:c.1137-225G>A	ENSP00000492014.1:n.1137-225G>A
ENST00000053867.7:c.1414-37G>A	ENSP00000053867.2:n.1414-37G>A
ENST00000586242.1:c.48-37G>A
ENST00000586443.1:c.855-37G>A
ENST00000589265.5:c.943-37G>A	ENSP00000467616.1:n.943-37G>A
NM_002087.3:c.1414-37G>A	NP_002078.1:n.1414-37G>A
XM_005257253.1:c.1414-37G>A	XP_005257310.1:n.1414-37G>A
XM_024450730.1:c.1414-37G>A	XP_024306498.1:n.1414-37G>A
NM_002087.4:c.1414-37G>A MANE Select	NP_002078.1:n.1414-37G>A