Canonical Allele Identifier: CA2261354280

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351697_44351699delinsAAG , CM000679.2:g.44351697_44351699delinsAAG	GRCh38
NC_000017.10:g.42429065_42429067delinsAAG , CM000679.1:g.42429065_42429067delinsAAG	GRCh37
NC_000017.9:g.39784591_39784593delinsAAG	NCBI36
NG_007886.1:g.11575_11577delinsAAG , LRG_661:g.11575_11577delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1081_1083delinsAAG MANE Select	ENSP00000053867.2:p.Lys361=
ENST00000639447.1:c.1081_1083delinsAAG	ENSP00000492014.1:p.Lys361=
ENST00000053867.7:c.1081_1083delinsAAG	ENSP00000053867.2:p.Lys361=
ENST00000586443.1:c.522_524delinsAAG
ENST00000589265.5:c.610_612delinsAAG	ENSP00000467616.1:p.Lys204=
ENST00000589923.1:n.339_341delinsAAG
NM_002087.3:c.1081_1083delinsAAG	NP_002078.1:p.Lys361=
XM_005257253.1:c.1081_1083delinsAAG	XP_005257310.1:p.Lys361=
XM_024450730.1:c.1081_1083delinsAAG	XP_024306498.1:p.Lys361=
NM_002087.4:c.1081_1083delinsAAG MANE Select	NP_002078.1:p.Lys361=