Canonical Allele Identifier: CA2809588866

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351888dup , CM000679.2:g.44351888dup	GRCh38
NC_000017.10:g.42429256dup , CM000679.1:g.42429256dup	GRCh37
NC_000017.9:g.39784782dup	NCBI36
NG_007886.1:g.11766dup , LRG_661:g.11766dup

Transcript Alleles

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