Canonical Allele Identifier: CA2809588883

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352261_44352262insACT , CM000679.2:g.44352261_44352262insACT	GRCh38
NC_000017.10:g.42429629_42429630insACT , CM000679.1:g.42429629_42429630insACT	GRCh37
NC_000017.9:g.39785155_39785156insACT	NCBI36
NG_007886.1:g.12139_12140insACT , LRG_661:g.12139_12140insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1413+13_1413+14insACT MANE Select	ENSP00000053867.2:n.1413+13_1413+14insACT
ENST00000639447.1:c.1137-268_1137-267insACT	ENSP00000492014.1:n.1137-268_1137-267insACT
ENST00000053867.7:c.1413+13_1413+14insACT	ENSP00000053867.2:n.1413+13_1413+14insACT
ENST00000586242.1:c.47+13_47+14insACT
ENST00000586443.1:c.854+13_854+14insACT
ENST00000589265.5:c.942+13_942+14insACT	ENSP00000467616.1:n.942+13_942+14insACT
NM_002087.3:c.1413+13_1413+14insACT	NP_002078.1:n.1413+13_1413+14insACT
XM_005257253.1:c.1413+13_1413+14insACT	XP_005257310.1:n.1413+13_1413+14insACT
XM_024450730.1:c.1413+13_1413+14insACT	XP_024306498.1:n.1413+13_1413+14insACT
NM_002087.4:c.1413+13_1413+14insACT MANE Select	NP_002078.1:n.1413+13_1413+14insACT