Canonical Allele Identifier: CA2579758278

Gene: GRN

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1317del MANE Select	ENSP00000053867.2:p.Arg440GlufsTer?
ENST00000639447.1:c.1137-377del	ENSP00000492014.1:n.1137-377del
ENST00000053867.7:c.1317del	ENSP00000053867.2:p.Arg440GlufsTer?
ENST00000586443.1:c.758del
ENST00000589265.5:c.846del	ENSP00000467616.1:p.Arg283GlufsTer?
NM_002087.3:c.1317del	NP_002078.1:p.Arg440GlufsTer?
XM_005257253.1:c.1317del	XP_005257310.1:p.Arg440GlufsTer?
XM_024450730.1:c.1317del	XP_024306498.1:p.Arg440GlufsTer?
NM_002087.4:c.1317del MANE Select	NP_002078.1:p.Arg440GlufsTer?