Canonical Allele Identifier: CA983971312

Gene: GRN

Linked Data

• dbSNP Id: rs2048378194
• gnomAD v3: 17-44351832-T-G
• gnomAD v4: 17-44351832-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351832T>G , CM000679.2:g.44351832T>G	GRCh38
NC_000017.10:g.42429200T>G , CM000679.1:g.42429200T>G	GRCh37
NC_000017.9:g.39784726T>G	NCBI36
NG_007886.1:g.11710T>G , LRG_661:g.11710T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+37T>G MANE Select	ENSP00000053867.2:n.1179+37T>G
ENST00000639447.1:c.1136+80T>G	ENSP00000492014.1:n.1136+80T>G
ENST00000053867.7:c.1179+37T>G	ENSP00000053867.2:n.1179+37T>G
ENST00000586443.1:c.620+37T>G
ENST00000589265.5:c.708+37T>G	ENSP00000467616.1:n.708+37T>G
NM_002087.3:c.1179+37T>G	NP_002078.1:n.1179+37T>G
XM_005257253.1:c.1179+37T>G	XP_005257310.1:n.1179+37T>G
XM_024450730.1:c.1179+37T>G	XP_024306498.1:n.1179+37T>G
NM_002087.4:c.1179+37T>G MANE Select	NP_002078.1:n.1179+37T>G