Canonical Allele Identifier: CA2576290524

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351704_44351728del , CM000679.2:g.44351704_44351728del	GRCh38
NC_000017.10:g.42429072_42429096del , CM000679.1:g.42429072_42429096del	GRCh37
NC_000017.9:g.39784598_39784622del	NCBI36
NG_007886.1:g.11582_11606del , LRG_661:g.11582_11606del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1088_1112del MANE Select	ENSP00000053867.2:p.Asp363AlafsTer?
ENST00000639447.1:c.1088_1112del	ENSP00000492014.1:p.Asp363AlafsTer?
ENST00000053867.7:c.1088_1112del	ENSP00000053867.2:p.Asp363AlafsTer?
ENST00000586443.1:c.529_553del
ENST00000589265.5:c.617_641del	ENSP00000467616.1:p.Asp206AlafsTer?
ENST00000589923.1:n.346_370del
NM_002087.3:c.1088_1112del	NP_002078.1:p.Asp363AlafsTer?
XM_005257253.1:c.1088_1112del	XP_005257310.1:p.Asp363AlafsTer?
XM_024450730.1:c.1088_1112del	XP_024306498.1:p.Asp363AlafsTer?
NM_002087.4:c.1088_1112del MANE Select	NP_002078.1:p.Asp363AlafsTer?