Canonical Allele Identifier: CA2733703908
Gene: GRN HGNC NCBI

Linked Data

dbSNP Id: rs2143342470

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44351796_44351797insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC , CM000679.2:g.44351796_44351797insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC GRCh38
NC_000017.10:g.42429164_42429165insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC , CM000679.1:g.42429164_42429165insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC GRCh37
NC_000017.9:g.39784690_39784691insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC NCBI36
NG_007886.1:g.11674_11675insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC , LRG_661:g.11674_11675insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC MANE Select ENSP00000053867.2:n.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCA...
ENST00000639447.1:c.1136+44_1136+45insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC ENSP00000492014.1:n.1136+44_1136+45insCTGTCTGCTGCTCGGACCACCAG...
ENST00000053867.7:c.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC ENSP00000053867.2:n.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCA...
ENST00000586443.1:c.620+1_620+2insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC
ENST00000589265.5:c.708+1_708+2insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC ENSP00000467616.1:n.708+1_708+2insCTGTCTGCTGCTCGGACCACCAGCACT...
NM_002087.3:c.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC NP_002078.1:n.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCACTGCTG...
XM_005257253.1:c.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC XP_005257310.1:n.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCACTG...
XM_024450730.1:c.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC XP_024306498.1:n.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCACTG...
NM_002087.4:c.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCACTGCTGCCCCCAGGGC MANE Select NP_002078.1:n.1179+1_1179+2insCTGTCTGCTGCTCGGACCACCAGCACTGCTG...