Canonical Allele Identifier: CA2638210943

Gene: GRN

Linked Data

• dbSNP Id: rs2143346858
• gnomAD v4: 17-44352331-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352335dup , CM000679.2:g.44352335dup	GRCh38
NC_000017.10:g.42429703dup , CM000679.1:g.42429703dup	GRCh37
NC_000017.9:g.39785229dup	NCBI36
NG_007886.1:g.12213dup , LRG_661:g.12213dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1414-6dup MANE Select	ENSP00000053867.2:n.1414-6dup
ENST00000639447.1:c.1137-194dup	ENSP00000492014.1:n.1137-194dup
ENST00000053867.7:c.1414-6dup	ENSP00000053867.2:n.1414-6dup
ENST00000586242.1:c.48-6dup
ENST00000586443.1:c.855-6dup
ENST00000589265.5:c.943-6dup	ENSP00000467616.1:n.943-6dup
NM_002087.3:c.1414-6dup	NP_002078.1:n.1414-6dup
XM_005257253.1:c.1414-6dup	XP_005257310.1:n.1414-6dup
XM_024450730.1:c.1414-6dup	XP_024306498.1:n.1414-6dup
NM_002087.4:c.1414-6dup MANE Select	NP_002078.1:n.1414-6dup