Canonical Allele Identifier: CA2809588848

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351839_44351840insA , CM000679.2:g.44351839_44351840insA	GRCh38
NC_000017.10:g.42429207_42429208insA , CM000679.1:g.42429207_42429208insA	GRCh37
NC_000017.9:g.39784733_39784734insA	NCBI36
NG_007886.1:g.11717_11718insA , LRG_661:g.11717_11718insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+44_1179+45insA MANE Select	ENSP00000053867.2:n.1179+44_1179+45insA
ENST00000639447.1:c.1136+87_1136+88insA	ENSP00000492014.1:n.1136+87_1136+88insA
ENST00000053867.7:c.1179+44_1179+45insA	ENSP00000053867.2:n.1179+44_1179+45insA
ENST00000586443.1:c.620+44_620+45insA
ENST00000589265.5:c.708+44_708+45insA	ENSP00000467616.1:n.708+44_708+45insA
NM_002087.3:c.1179+44_1179+45insA	NP_002078.1:n.1179+44_1179+45insA
XM_005257253.1:c.1179+44_1179+45insA	XP_005257310.1:n.1179+44_1179+45insA
XM_024450730.1:c.1179+44_1179+45insA	XP_024306498.1:n.1179+44_1179+45insA
NM_002087.4:c.1179+44_1179+45insA MANE Select	NP_002078.1:n.1179+44_1179+45insA