Canonical Allele Identifier: CA2638210027

Gene: GRN

Linked Data

• gnomAD v4: 17-44351900-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351900_44351901insA , CM000679.2:g.44351900_44351901insA	GRCh38
NC_000017.10:g.42429268_42429269insA , CM000679.1:g.42429268_42429269insA	GRCh37
NC_000017.9:g.39784794_39784795insA	NCBI36
NG_007886.1:g.11778_11779insA , LRG_661:g.11778_11779insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+105_1179+106insA MANE Select	ENSP00000053867.2:n.1179+105_1179+106insA
ENST00000639447.1:c.1136+148_1136+149insA	ENSP00000492014.1:n.1136+148_1136+149insA
ENST00000053867.7:c.1179+105_1179+106insA	ENSP00000053867.2:n.1179+105_1179+106insA
ENST00000586443.1:c.620+105_620+106insA
ENST00000589265.5:c.708+105_708+106insA	ENSP00000467616.1:n.708+105_708+106insA
NM_002087.3:c.1179+105_1179+106insA	NP_002078.1:n.1179+105_1179+106insA
XM_005257253.1:c.1179+105_1179+106insA	XP_005257310.1:n.1179+105_1179+106insA
XM_024450730.1:c.1179+105_1179+106insA	XP_024306498.1:n.1179+105_1179+106insA
NM_002087.4:c.1179+105_1179+106insA MANE Select	NP_002078.1:n.1179+105_1179+106insA