Canonical Allele Identifier: CA2638209707

Gene: GRN

Linked Data

• gnomAD v4: 17-44351671-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351672dup , CM000679.2:g.44351672dup	GRCh38
NC_000017.10:g.42429040dup , CM000679.1:g.42429040dup	GRCh37
NC_000017.9:g.39784566dup	NCBI36
NG_007886.1:g.11550dup , LRG_661:g.11550dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1056dup MANE Select	ENSP00000053867.2:p.Ser353GlnfsTer15
ENST00000639447.1:c.1056dup	ENSP00000492014.1:p.Ser353GlnfsTer15
ENST00000053867.7:c.1056dup	ENSP00000053867.2:p.Ser353GlnfsTer15
ENST00000586443.1:c.497dup
ENST00000589265.5:c.585dup	ENSP00000467616.1:p.Ser196GlnfsTer15
ENST00000589923.1:n.314dup
NM_002087.3:c.1056dup	NP_002078.1:p.Ser353GlnfsTer15
XM_005257253.1:c.1056dup	XP_005257310.1:p.Ser353GlnfsTer15
XM_024450730.1:c.1056dup	XP_024306498.1:p.Ser353GlnfsTer15
NM_002087.4:c.1056dup MANE Select	NP_002078.1:p.Ser353GlnfsTer15