Canonical Allele Identifier: CA2638210599

Gene: GRN

Linked Data

• gnomAD v4: 17-44352191-GGGGCAGACCTGCTGCCCGAGCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352195_44352217del , CM000679.2:g.44352195_44352217del	GRCh38
NC_000017.10:g.42429563_42429585del , CM000679.1:g.42429563_42429585del	GRCh37
NC_000017.9:g.39785089_39785111del	NCBI36
NG_007886.1:g.12073_12095del , LRG_661:g.12073_12095del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1360_1382del MANE Select	ENSP00000053867.2:p.Gln454TrpfsTer?
ENST00000639447.1:c.1137-334_1137-312del	ENSP00000492014.1:n.1137-334_1137-312del
ENST00000053867.7:c.1360_1382del	ENSP00000053867.2:p.Gln454TrpfsTer?
ENST00000586443.1:c.801_823del
ENST00000589265.5:c.889_911del	ENSP00000467616.1:p.Gln297TrpfsTer?
NM_002087.3:c.1360_1382del	NP_002078.1:p.Gln454TrpfsTer?
XM_005257253.1:c.1360_1382del	XP_005257310.1:p.Gln454TrpfsTer?
XM_024450730.1:c.1360_1382del	XP_024306498.1:p.Gln454TrpfsTer?
NM_002087.4:c.1360_1382del MANE Select	NP_002078.1:p.Gln454TrpfsTer?