Canonical Allele Identifier: CA2809588877

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352087_44352088del , CM000679.2:g.44352087_44352088del	GRCh38
NC_000017.10:g.42429455_42429456del , CM000679.1:g.42429455_42429456del	GRCh37
NC_000017.9:g.39784981_39784982del	NCBI36
NG_007886.1:g.11965_11966del , LRG_661:g.11965_11966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1252_1253del MANE Select	ENSP00000053867.2:p.Gly419LysfsTer26
ENST00000639447.1:c.1136+335_1136+336del	ENSP00000492014.1:n.1136+335_1136+336del
ENST00000053867.7:c.1252_1253del	ENSP00000053867.2:p.Gly419LysfsTer26
ENST00000586443.1:c.693_694del
ENST00000589265.5:c.781_782del	ENSP00000467616.1:p.Gly262LysfsTer26
NM_002087.3:c.1252_1253del	NP_002078.1:p.Gly419LysfsTer26
XM_005257253.1:c.1252_1253del	XP_005257310.1:p.Gly419LysfsTer26
XM_024450730.1:c.1252_1253del	XP_024306498.1:p.Gly419LysfsTer26
NM_002087.4:c.1252_1253del MANE Select	NP_002078.1:p.Gly419LysfsTer26