Canonical Allele Identifier: CA2695226237

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352031_44352032del , CM000679.2:g.44352031_44352032del	GRCh38
NC_000017.10:g.42429399_42429400del , CM000679.1:g.42429399_42429400del	GRCh37
NC_000017.9:g.39784925_39784926del	NCBI36
NG_007886.1:g.11909_11910del , LRG_661:g.11909_11910del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1196_1197del MANE Select	ENSP00000053867.2:p.Asp399AlafsTer14
ENST00000639447.1:c.1136+279_1136+280del	ENSP00000492014.1:n.1136+279_1136+280del
ENST00000053867.7:c.1196_1197del	ENSP00000053867.2:p.Asp399AlafsTer14
ENST00000586443.1:c.637_638del
ENST00000589265.5:c.725_726del	ENSP00000467616.1:p.Asp242AlafsTer14
NM_002087.3:c.1196_1197del	NP_002078.1:p.Asp399AlafsTer14
XM_005257253.1:c.1196_1197del	XP_005257310.1:p.Asp399AlafsTer14
XM_024450730.1:c.1196_1197del	XP_024306498.1:p.Asp399AlafsTer14
NM_002087.4:c.1196_1197del MANE Select	NP_002078.1:p.Asp399AlafsTer14