Canonical Allele Identifier: CA2261354286

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351710_44351712delinsCCT , CM000679.2:g.44351710_44351712delinsCCT	GRCh38
NC_000017.10:g.42429078_42429080delinsCCT , CM000679.1:g.42429078_42429080delinsCCT	GRCh37
NC_000017.9:g.39784604_39784606delinsCCT	NCBI36
NG_007886.1:g.11588_11590delinsCCT , LRG_661:g.11588_11590delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1094_1096delinsCCT MANE Select	ENSP00000053867.2:p.Pro365=
ENST00000639447.1:c.1094_1096delinsCCT	ENSP00000492014.1:p.Pro365=
ENST00000053867.7:c.1094_1096delinsCCT	ENSP00000053867.2:p.Pro365=
ENST00000586443.1:c.535_537delinsCCT
ENST00000589265.5:c.623_625delinsCCT	ENSP00000467616.1:p.Pro208=
ENST00000589923.1:n.352_354delinsCCT
NM_002087.3:c.1094_1096delinsCCT	NP_002078.1:p.Pro365=
XM_005257253.1:c.1094_1096delinsCCT	XP_005257310.1:p.Pro365=
XM_024450730.1:c.1094_1096delinsCCT	XP_024306498.1:p.Pro365=
NM_002087.4:c.1094_1096delinsCCT MANE Select	NP_002078.1:p.Pro365=