Canonical Allele Identifier: CA399769180

Gene: GRN

Linked Data

• dbSNP Id: rs2048383083
• MyVariant Identifiers: chr17:g.42429561G>T (hg19) ; chr17:g.44352193G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352193G>T , CM000679.2:g.44352193G>T	GRCh38
NC_000017.10:g.42429561G>T , CM000679.1:g.42429561G>T	GRCh37
NC_000017.9:g.39785087G>T	NCBI36
NG_007886.1:g.12071G>T , LRG_661:g.12071G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1358G>T MANE Select	ENSP00000053867.2:p.Gly453Val
ENST00000639447.1:c.1137-336G>T	ENSP00000492014.1:n.1137-336G>T
ENST00000053867.7:c.1358G>T	ENSP00000053867.2:p.Gly453Val
ENST00000586443.1:c.799G>T
ENST00000589265.5:c.887G>T	ENSP00000467616.1:p.Gly296Val
NM_002087.3:c.1358G>T	NP_002078.1:p.Gly453Val
XM_005257253.1:c.1358G>T	XP_005257310.1:p.Gly453Val
XM_024450730.1:c.1358G>T	XP_024306498.1:p.Gly453Val
NM_002087.4:c.1358G>T MANE Select	NP_002078.1:p.Gly453Val