Canonical Allele Identifier: CA2576290563

Gene: GRN

Linked Data

• ClinVar Variation Id: 2925625
• ClinVar RCV Id: RCV003783719

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352152_44352153del , CM000679.2:g.44352152_44352153del	GRCh38
NC_000017.10:g.42429520_42429521del , CM000679.1:g.42429520_42429521del	GRCh37
NC_000017.9:g.39785046_39785047del	NCBI36
NG_007886.1:g.12030_12031del , LRG_661:g.12030_12031del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1317_1318del MANE Select	ENSP00000053867.2:p.Asp441HisfsTer4
ENST00000639447.1:c.1137-377_1137-376del	ENSP00000492014.1:n.1137-377_1137-376del
ENST00000053867.7:c.1317_1318del	ENSP00000053867.2:p.Asp441HisfsTer4
ENST00000586443.1:c.758_759del
ENST00000589265.5:c.846_847del	ENSP00000467616.1:p.Asp284HisfsTer4
NM_002087.3:c.1317_1318del	NP_002078.1:p.Asp441HisfsTer4
XM_005257253.1:c.1317_1318del	XP_005257310.1:p.Asp441HisfsTer4
XM_024450730.1:c.1317_1318del	XP_024306498.1:p.Asp441HisfsTer4
NM_002087.4:c.1317_1318del MANE Select	NP_002078.1:p.Asp441HisfsTer4