Canonical Allele Identifier: CA2261354608

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352324_44352329delinsGCTCCC , CM000679.2:g.44352324_44352329delinsGCTCCC	GRCh38
NC_000017.10:g.42429692_42429697delinsGCTCCC , CM000679.1:g.42429692_42429697delinsGCTCCC	GRCh37
NC_000017.9:g.39785218_39785223delinsGCTCCC	NCBI36
NG_007886.1:g.12202_12207delinsGCTCCC , LRG_661:g.12202_12207delinsGCTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1414-17_1414-12delinsGCTCCC MANE Select	ENSP00000053867.2:n.1414-17_1414-12delinsGCTCCC
ENST00000639447.1:c.1137-205_1137-200delinsGCTCCC	ENSP00000492014.1:n.1137-205_1137-200delinsGCTCCC
ENST00000053867.7:c.1414-17_1414-12delinsGCTCCC	ENSP00000053867.2:n.1414-17_1414-12delinsGCTCCC
ENST00000586242.1:c.48-17_48-12delinsGCTCCC
ENST00000586443.1:c.855-17_855-12delinsGCTCCC
ENST00000589265.5:c.943-17_943-12delinsGCTCCC	ENSP00000467616.1:n.943-17_943-12delinsGCTCCC
NM_002087.3:c.1414-17_1414-12delinsGCTCCC	NP_002078.1:n.1414-17_1414-12delinsGCTCCC
XM_005257253.1:c.1414-17_1414-12delinsGCTCCC	XP_005257310.1:n.1414-17_1414-12delinsGCTCCC
XM_024450730.1:c.1414-17_1414-12delinsGCTCCC	XP_024306498.1:n.1414-17_1414-12delinsGCTCCC
NM_002087.4:c.1414-17_1414-12delinsGCTCCC MANE Select	NP_002078.1:n.1414-17_1414-12delinsGCTCCC