Canonical Allele Identifier: CA2638209702

Gene: GRN

Linked Data

• gnomAD v4: 17-44351663-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351664dup , CM000679.2:g.44351664dup	GRCh38
NC_000017.10:g.42429032dup , CM000679.1:g.42429032dup	GRCh37
NC_000017.9:g.39784558dup	NCBI36
NG_007886.1:g.11542dup , LRG_661:g.11542dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1048dup MANE Select	ENSP00000053867.2:p.Ala350GlyfsTer18
ENST00000639447.1:c.1048dup	ENSP00000492014.1:p.Ala350GlyfsTer18
ENST00000053867.7:c.1048dup	ENSP00000053867.2:p.Ala350GlyfsTer18
ENST00000586443.1:c.489dup
ENST00000589265.5:c.577dup	ENSP00000467616.1:p.Ala193GlyfsTer18
ENST00000589923.1:n.306dup
NM_002087.3:c.1048dup	NP_002078.1:p.Ala350GlyfsTer18
XM_005257253.1:c.1048dup	XP_005257310.1:p.Ala350GlyfsTer18
XM_024450730.1:c.1048dup	XP_024306498.1:p.Ala350GlyfsTer18
NM_002087.4:c.1048dup MANE Select	NP_002078.1:p.Ala350GlyfsTer18