Canonical Allele Identifier: CA2261354302

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351733_44351736delinsCCCT , CM000679.2:g.44351733_44351736delinsCCCT	GRCh38
NC_000017.10:g.42429101_42429104delinsCCCT , CM000679.1:g.42429101_42429104delinsCCCT	GRCh37
NC_000017.9:g.39784627_39784630delinsCCCT	NCBI36
NG_007886.1:g.11611_11614delinsCCCT , LRG_661:g.11611_11614delinsCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1117_1120delinsCCCT MANE Select	ENSP00000053867.2:p.Pro373=
ENST00000639447.1:c.1117_1120delinsCCCT	ENSP00000492014.1:p.Pro373=
ENST00000053867.7:c.1117_1120delinsCCCT	ENSP00000053867.2:p.Pro373=
ENST00000586443.1:c.558_561delinsCCCT
ENST00000589265.5:c.646_649delinsCCCT	ENSP00000467616.1:p.Pro216=
ENST00000589923.1:n.375_378delinsCCCT
NM_002087.3:c.1117_1120delinsCCCT	NP_002078.1:p.Pro373=
XM_005257253.1:c.1117_1120delinsCCCT	XP_005257310.1:p.Pro373=
XM_024450730.1:c.1117_1120delinsCCCT	XP_024306498.1:p.Pro373=
NM_002087.4:c.1117_1120delinsCCCT MANE Select	NP_002078.1:p.Pro373=