Canonical Allele Identifier: CA2261354535

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352180_44352201delinsAGCTGCCCGGTGGGGCAGACCT , CM000679.2:g.44352180_44352201delinsAGCTGCCCGGTGGGGCAGACCT	GRCh38
NC_000017.10:g.42429548_42429569delinsAGCTGCCCGGTGGGGCAGACCT , CM000679.1:g.42429548_42429569delinsAGCTGCCCGGTGGGGCAGACCT	GRCh37
NC_000017.9:g.39785074_39785095delinsAGCTGCCCGGTGGGGCAGACCT	NCBI36
NG_007886.1:g.12058_12079delinsAGCTGCCCGGTGGGGCAGACCT , LRG_661:g.12058_12079delinsAGCTGCCCGGTGGGGCAGACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1345_1366delinsAGCTGCCCGGTGGGGCAGACCT MANE Select	ENSP00000053867.2:p.Ser449=
ENST00000639447.1:c.1137-349_1137-328delinsAGCTGCCCGGTGGGGCAGACCT	ENSP00000492014.1:n.1137-349_1137-328delinsAGCTGCCCGGTGGGGCAG...
ENST00000053867.7:c.1345_1366delinsAGCTGCCCGGTGGGGCAGACCT	ENSP00000053867.2:p.Ser449=
ENST00000586443.1:c.786_807delinsAGCTGCCCGGTGGGGCAGACCT
ENST00000589265.5:c.874_895delinsAGCTGCCCGGTGGGGCAGACCT	ENSP00000467616.1:p.Ser292=
NM_002087.3:c.1345_1366delinsAGCTGCCCGGTGGGGCAGACCT	NP_002078.1:p.Ser449=
XM_005257253.1:c.1345_1366delinsAGCTGCCCGGTGGGGCAGACCT	XP_005257310.1:p.Ser449=
XM_024450730.1:c.1345_1366delinsAGCTGCCCGGTGGGGCAGACCT	XP_024306498.1:p.Ser449=
NM_002087.4:c.1345_1366delinsAGCTGCCCGGTGGGGCAGACCT MANE Select	NP_002078.1:p.Ser449=