Canonical Allele Identifier: CA2261354579

Gene: GRN

Linked Data

• dbSNP Id: rs776817374

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352274G>T , CM000679.2:g.44352274G>T	GRCh38
NC_000017.10:g.42429642G>T , CM000679.1:g.42429642G>T	GRCh37
NC_000017.9:g.39785168G>T	NCBI36
NG_007886.1:g.12152G>T , LRG_661:g.12152G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1413+26G>T MANE Select	ENSP00000053867.2:n.1413+26G>T
ENST00000639447.1:c.1137-255G>T	ENSP00000492014.1:n.1137-255G>T
ENST00000053867.7:c.1413+26G>T	ENSP00000053867.2:n.1413+26G>T
ENST00000586242.1:c.47+26G>T
ENST00000586443.1:c.854+26G>T
ENST00000589265.5:c.942+26G>T	ENSP00000467616.1:n.942+26G>T
NM_002087.3:c.1413+26G>T	NP_002078.1:n.1413+26G>T
XM_005257253.1:c.1413+26G>T	XP_005257310.1:n.1413+26G>T
XM_024450730.1:c.1413+26G>T	XP_024306498.1:n.1413+26G>T
NM_002087.4:c.1413+26G>T MANE Select	NP_002078.1:n.1413+26G>T