Canonical Allele Identifier: CA2837994618

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352114_44352116del , CM000679.2:g.44352114_44352116del	GRCh38
NC_000017.10:g.42429482_42429484del , CM000679.1:g.42429482_42429484del	GRCh37
NC_000017.9:g.39785008_39785010del	NCBI36
NG_007886.1:g.11992_11994del , LRG_661:g.11992_11994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1279_1281del MANE Select	ENSP00000053867.2:p.Glu427del
ENST00000639447.1:c.1136+362_1136+364del	ENSP00000492014.1:n.1136+362_1136+364del
ENST00000053867.7:c.1279_1281del	ENSP00000053867.2:p.Glu427del
ENST00000586443.1:c.720_722del
ENST00000589265.5:c.808_810del	ENSP00000467616.1:p.Glu270del
NM_002087.3:c.1279_1281del	NP_002078.1:p.Glu427del
XM_005257253.1:c.1279_1281del	XP_005257310.1:p.Glu427del
XM_024450730.1:c.1279_1281del	XP_024306498.1:p.Glu427del
NM_002087.4:c.1279_1281del MANE Select	NP_002078.1:p.Glu427del