Canonical Allele Identifier: CA399768429

Gene: GRN

Linked Data

• gnomAD v4: 17-44352067-T-G
• MyVariant Identifiers: chr17:g.42429435T>G (hg19) ; chr17:g.44352067T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352067T>G , CM000679.2:g.44352067T>G	GRCh38
NC_000017.10:g.42429435T>G , CM000679.1:g.42429435T>G	GRCh37
NC_000017.9:g.39784961T>G	NCBI36
NG_007886.1:g.11945T>G , LRG_661:g.11945T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1232T>G MANE Select	ENSP00000053867.2:p.Val411Gly
ENST00000639447.1:c.1136+315T>G	ENSP00000492014.1:n.1136+315T>G
ENST00000053867.7:c.1232T>G	ENSP00000053867.2:p.Val411Gly
ENST00000586443.1:c.673T>G
ENST00000589265.5:c.761T>G	ENSP00000467616.1:p.Val254Gly
NM_002087.3:c.1232T>G	NP_002078.1:p.Val411Gly
XM_005257253.1:c.1232T>G	XP_005257310.1:p.Val411Gly
XM_024450730.1:c.1232T>G	XP_024306498.1:p.Val411Gly
NM_002087.4:c.1232T>G MANE Select	NP_002078.1:p.Val411Gly