Canonical Allele Identifier: CA2261354586

Gene: GRN

Linked Data

• dbSNP Id: rs2048384155

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352282A>T , CM000679.2:g.44352282A>T	GRCh38
NC_000017.10:g.42429650A>T , CM000679.1:g.42429650A>T	GRCh37
NC_000017.9:g.39785176A>T	NCBI36
NG_007886.1:g.12160A>T , LRG_661:g.12160A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1413+34A>T MANE Select	ENSP00000053867.2:n.1413+34A>T
ENST00000639447.1:c.1137-247A>T	ENSP00000492014.1:n.1137-247A>T
ENST00000053867.7:c.1413+34A>T	ENSP00000053867.2:n.1413+34A>T
ENST00000586242.1:c.47+34A>T
ENST00000586443.1:c.854+34A>T
ENST00000589265.5:c.942+34A>T	ENSP00000467616.1:n.942+34A>T
NM_002087.3:c.1413+34A>T	NP_002078.1:n.1413+34A>T
XM_005257253.1:c.1413+34A>T	XP_005257310.1:n.1413+34A>T
XM_024450730.1:c.1413+34A>T	XP_024306498.1:n.1413+34A>T
NM_002087.4:c.1413+34A>T MANE Select	NP_002078.1:n.1413+34A>T