Canonical Allele Identifier: CA2809588849

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351842del , CM000679.2:g.44351842del	GRCh38
NC_000017.10:g.42429210del , CM000679.1:g.42429210del	GRCh37
NC_000017.9:g.39784736del	NCBI36
NG_007886.1:g.11720del , LRG_661:g.11720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+47del MANE Select	ENSP00000053867.2:n.1179+47del
ENST00000639447.1:c.1136+90del	ENSP00000492014.1:n.1136+90del
ENST00000053867.7:c.1179+47del	ENSP00000053867.2:n.1179+47del
ENST00000586443.1:c.620+47del
ENST00000589265.5:c.708+47del	ENSP00000467616.1:n.708+47del
NM_002087.3:c.1179+47del	NP_002078.1:n.1179+47del
XM_005257253.1:c.1179+47del	XP_005257310.1:n.1179+47del
XM_024450730.1:c.1179+47del	XP_024306498.1:n.1179+47del
NM_002087.4:c.1179+47del MANE Select	NP_002078.1:n.1179+47del