Canonical Allele Identifier: CA2638209726

Gene: GRN

Linked Data

• gnomAD v4: 17-44351683-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351686del , CM000679.2:g.44351686del	GRCh38
NC_000017.10:g.42429054del , CM000679.1:g.42429054del	GRCh37
NC_000017.9:g.39784580del	NCBI36
NG_007886.1:g.11564del , LRG_661:g.11564del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1070del MANE Select	ENSP00000053867.2:p.Pro357HisfsTer4
ENST00000639447.1:c.1070del	ENSP00000492014.1:p.Pro357HisfsTer4
ENST00000053867.7:c.1070del	ENSP00000053867.2:p.Pro357HisfsTer4
ENST00000586443.1:c.511del
ENST00000589265.5:c.599del	ENSP00000467616.1:p.Pro200HisfsTer4
ENST00000589923.1:n.328del
NM_002087.3:c.1070del	NP_002078.1:p.Pro357HisfsTer4
XM_005257253.1:c.1070del	XP_005257310.1:p.Pro357HisfsTer4
XM_024450730.1:c.1070del	XP_024306498.1:p.Pro357HisfsTer4
NM_002087.4:c.1070del MANE Select	NP_002078.1:p.Pro357HisfsTer4