Canonical Allele Identifier: CA2261354547

Gene: GRN

Linked Data

• dbSNP Id: rs2048383162

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352204_44352206dup , CM000679.2:g.44352204_44352206dup	GRCh38
NC_000017.10:g.42429572_42429574dup , CM000679.1:g.42429572_42429574dup	GRCh37
NC_000017.9:g.39785098_39785100dup	NCBI36
NG_007886.1:g.12082_12084dup , LRG_661:g.12082_12084dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1369_1371dup MANE Select	ENSP00000053867.2:p.Cys457_Pro458insCys
ENST00000639447.1:c.1137-325_1137-323dup	ENSP00000492014.1:n.1137-325_1137-323dup
ENST00000053867.7:c.1369_1371dup	ENSP00000053867.2:p.Cys457_Pro458insCys
ENST00000586443.1:c.810_812dup
ENST00000589265.5:c.898_900dup	ENSP00000467616.1:p.Cys300_Pro301insCys
NM_002087.3:c.1369_1371dup	NP_002078.1:p.Cys457_Pro458insCys
XM_005257253.1:c.1369_1371dup	XP_005257310.1:p.Cys457_Pro458insCys
XM_024450730.1:c.1369_1371dup	XP_024306498.1:p.Cys457_Pro458insCys
NM_002087.4:c.1369_1371dup MANE Select	NP_002078.1:p.Cys457_Pro458insCys