Canonical Allele Identifier: CA2695226232

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351761_44351762insA , CM000679.2:g.44351761_44351762insA	GRCh38
NC_000017.10:g.42429129_42429130insA , CM000679.1:g.42429129_42429130insA	GRCh37
NC_000017.9:g.39784655_39784656insA	NCBI36
NG_007886.1:g.11639_11640insA , LRG_661:g.11639_11640insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1145_1146insA MANE Select	ENSP00000053867.2:p.Ser383ValfsTer?
ENST00000639447.1:c.1136+9_1136+10insA	ENSP00000492014.1:n.1136+9_1136+10insA
ENST00000053867.7:c.1145_1146insA	ENSP00000053867.2:p.Ser383ValfsTer?
ENST00000586443.1:c.586_587insA
ENST00000589265.5:c.674_675insA	ENSP00000467616.1:p.Ser226ValfsTer?
ENST00000589923.1:n.403_404insA
NM_002087.3:c.1145_1146insA	NP_002078.1:p.Ser383ValfsTer?
XM_005257253.1:c.1145_1146insA	XP_005257310.1:p.Ser383ValfsTer?
XM_024450730.1:c.1145_1146insA	XP_024306498.1:p.Ser383ValfsTer?
NM_002087.4:c.1145_1146insA MANE Select	NP_002078.1:p.Ser383ValfsTer?