Canonical Allele Identifier: CA2638209990

Gene: GRN

Linked Data

• gnomAD v4: 17-44351871-G-GCCCATAGGTGATA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351876_44351888dup , CM000679.2:g.44351876_44351888dup	GRCh38
NC_000017.10:g.42429244_42429256dup , CM000679.1:g.42429244_42429256dup	GRCh37
NC_000017.9:g.39784770_39784782dup	NCBI36
NG_007886.1:g.11754_11766dup , LRG_661:g.11754_11766dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+81_1179+93dup MANE Select	ENSP00000053867.2:n.1179+81_1179+93dup
ENST00000639447.1:c.1136+124_1136+136dup	ENSP00000492014.1:n.1136+124_1136+136dup
ENST00000053867.7:c.1179+81_1179+93dup	ENSP00000053867.2:n.1179+81_1179+93dup
ENST00000586443.1:c.620+81_620+93dup
ENST00000589265.5:c.708+81_708+93dup	ENSP00000467616.1:n.708+81_708+93dup
NM_002087.3:c.1179+81_1179+93dup	NP_002078.1:n.1179+81_1179+93dup
XM_005257253.1:c.1179+81_1179+93dup	XP_005257310.1:n.1179+81_1179+93dup
XM_024450730.1:c.1179+81_1179+93dup	XP_024306498.1:n.1179+81_1179+93dup
NM_002087.4:c.1179+81_1179+93dup MANE Select	NP_002078.1:n.1179+81_1179+93dup