Canonical Allele Identifier: CA2638210295

Gene: GRN

Linked Data

• gnomAD v4: 17-44352019-TCTGCTGCTCGGACCACCAGCACTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352024_44352047del , CM000679.2:g.44352024_44352047del	GRCh38
NC_000017.10:g.42429392_42429415del , CM000679.1:g.42429392_42429415del	GRCh37
NC_000017.9:g.39784918_39784941del	NCBI36
NG_007886.1:g.11902_11925del , LRG_661:g.11902_11925del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1189_1212del MANE Select	ENSP00000053867.2:p.Cys397_Cys404del
ENST00000639447.1:c.1136+272_1136+295del	ENSP00000492014.1:n.1136+272_1136+295del
ENST00000053867.7:c.1189_1212del	ENSP00000053867.2:p.Cys397_Cys404del
ENST00000586443.1:c.630_653del
ENST00000589265.5:c.718_741del	ENSP00000467616.1:p.Cys240_Cys247del
NM_002087.3:c.1189_1212del	NP_002078.1:p.Cys397_Cys404del
XM_005257253.1:c.1189_1212del	XP_005257310.1:p.Cys397_Cys404del
XM_024450730.1:c.1189_1212del	XP_024306498.1:p.Cys397_Cys404del
NM_002087.4:c.1189_1212del MANE Select	NP_002078.1:p.Cys397_Cys404del