Canonical Allele Identifier: CA2261354247

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351625_44351627delinsCAG , CM000679.2:g.44351625_44351627delinsCAG	GRCh38
NC_000017.10:g.42428993_42428995delinsCAG , CM000679.1:g.42428993_42428995delinsCAG	GRCh37
NC_000017.9:g.39784519_39784521delinsCAG	NCBI36
NG_007886.1:g.11503_11505delinsCAG , LRG_661:g.11503_11505delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1009_1011delinsCAG MANE Select	ENSP00000053867.2:p.Gln337=
ENST00000639447.1:c.1009_1011delinsCAG	ENSP00000492014.1:p.Gln337=
ENST00000053867.7:c.1009_1011delinsCAG	ENSP00000053867.2:p.Gln337=
ENST00000586443.1:c.450_452delinsCAG
ENST00000589265.5:c.538_540delinsCAG	ENSP00000467616.1:p.Gln180=
ENST00000589923.1:n.267_269delinsCAG
NM_002087.3:c.1009_1011delinsCAG	NP_002078.1:p.Gln337=
XM_005257253.1:c.1009_1011delinsCAG	XP_005257310.1:p.Gln337=
XM_024450730.1:c.1009_1011delinsCAG	XP_024306498.1:p.Gln337=
NM_002087.4:c.1009_1011delinsCAG MANE Select	NP_002078.1:p.Gln337=