Canonical Allele Identifier: CA2261354417

Gene: GRN

Linked Data

• dbSNP Id: rs1598365387
• gnomAD v4: 17-44351950-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351950T>G , CM000679.2:g.44351950T>G	GRCh38
NC_000017.10:g.42429318T>G , CM000679.1:g.42429318T>G	GRCh37
NC_000017.9:g.39784844T>G	NCBI36
NG_007886.1:g.11828T>G , LRG_661:g.11828T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1180-65T>G MANE Select	ENSP00000053867.2:n.1180-65T>G
ENST00000639447.1:c.1136+198T>G	ENSP00000492014.1:n.1136+198T>G
ENST00000053867.7:c.1180-65T>G	ENSP00000053867.2:n.1180-65T>G
ENST00000586443.1:c.621-65T>G
ENST00000589265.5:c.709-65T>G	ENSP00000467616.1:n.709-65T>G
NM_002087.3:c.1180-65T>G	NP_002078.1:n.1180-65T>G
XM_005257253.1:c.1180-65T>G	XP_005257310.1:n.1180-65T>G
XM_024450730.1:c.1180-65T>G	XP_024306498.1:n.1180-65T>G
NM_002087.4:c.1180-65T>G MANE Select	NP_002078.1:n.1180-65T>G