Canonical Allele Identifier: CA2261354424

Gene: GRN

Linked Data

• dbSNP Id: rs574857626
• gnomAD v4: 17-44351966-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351966C>G , CM000679.2:g.44351966C>G	GRCh38
NC_000017.10:g.42429334C>G , CM000679.1:g.42429334C>G	GRCh37
NC_000017.9:g.39784860C>G	NCBI36
NG_007886.1:g.11844C>G , LRG_661:g.11844C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1180-49C>G MANE Select	ENSP00000053867.2:n.1180-49C>G
ENST00000639447.1:c.1136+214C>G	ENSP00000492014.1:n.1136+214C>G
ENST00000053867.7:c.1180-49C>G	ENSP00000053867.2:n.1180-49C>G
ENST00000586443.1:c.621-49C>G
ENST00000589265.5:c.709-49C>G	ENSP00000467616.1:n.709-49C>G
NM_002087.3:c.1180-49C>G	NP_002078.1:n.1180-49C>G
XM_005257253.1:c.1180-49C>G	XP_005257310.1:n.1180-49C>G
XM_024450730.1:c.1180-49C>G	XP_024306498.1:n.1180-49C>G
NM_002087.4:c.1180-49C>G MANE Select	NP_002078.1:n.1180-49C>G