Canonical Allele Identifier: CA399766522

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42429144G>A (hg19) ; chr17:g.44351776G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351776G>A , CM000679.2:g.44351776G>A	GRCh38
NC_000017.10:g.42429144G>A , CM000679.1:g.42429144G>A	GRCh37
NC_000017.9:g.39784670G>A	NCBI36
NG_007886.1:g.11654G>A , LRG_661:g.11654G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1160G>A MANE Select	ENSP00000053867.2:p.Gly387Asp
ENST00000639447.1:c.1136+24G>A	ENSP00000492014.1:n.1136+24G>A
ENST00000053867.7:c.1160G>A	ENSP00000053867.2:p.Gly387Asp
ENST00000586443.1:c.601G>A
ENST00000589265.5:c.689G>A	ENSP00000467616.1:p.Gly230Asp
ENST00000589923.1:n.418G>A
NM_002087.3:c.1160G>A	NP_002078.1:p.Gly387Asp
XM_005257253.1:c.1160G>A	XP_005257310.1:p.Gly387Asp
XM_024450730.1:c.1160G>A	XP_024306498.1:p.Gly387Asp
NM_002087.4:c.1160G>A MANE Select	NP_002078.1:p.Gly387Asp