Canonical Allele Identifier: CA2261354322

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351768_44351792delinsGGAGTGGGGCTGCTGTCCAATCCCA , CM000679.2:g.44351768_44351792delinsGGAGTGGGGCTGCTGTCCAATCCCA	GRCh38
NC_000017.10:g.42429136_42429160delinsGGAGTGGGGCTGCTGTCCAATCCCA , CM000679.1:g.42429136_42429160delinsGGAGTGGGGCTGCTGTCCAATCCCA	GRCh37
NC_000017.9:g.39784662_39784686delinsGGAGTGGGGCTGCTGTCCAATCCCA	NCBI36
NG_007886.1:g.11646_11670delinsGGAGTGGGGCTGCTGTCCAATCCCA , LRG_661:g.11646_11670delinsGGAGTGGGGCTGCTGTCCAATCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1152_1176delinsGGAGTGGGGCTGCTGTCCAATCCCA MANE Select	ENSP00000053867.2:p.Gly384=
ENST00000639447.1:c.1136+16_1136+40delinsGGAGTGGGGCTGCTGTCCAATCCCA	ENSP00000492014.1:n.1136+16_1136+40delinsGGAGTGGGGCTGCTGTCCAA...
ENST00000053867.7:c.1152_1176delinsGGAGTGGGGCTGCTGTCCAATCCCA	ENSP00000053867.2:p.Gly384=
ENST00000586443.1:c.593_617delinsGGAGTGGGGCTGCTGTCCAATCCCA
ENST00000589265.5:c.681_705delinsGGAGTGGGGCTGCTGTCCAATCCCA	ENSP00000467616.1:p.Gly227=
ENST00000589923.1:n.410_434delinsGGAGTGGGGCTGCTGTCCAATCCCA
NM_002087.3:c.1152_1176delinsGGAGTGGGGCTGCTGTCCAATCCCA	NP_002078.1:p.Gly384=
XM_005257253.1:c.1152_1176delinsGGAGTGGGGCTGCTGTCCAATCCCA	XP_005257310.1:p.Gly384=
XM_024450730.1:c.1152_1176delinsGGAGTGGGGCTGCTGTCCAATCCCA	XP_024306498.1:p.Gly384=
NM_002087.4:c.1152_1176delinsGGAGTGGGGCTGCTGTCCAATCCCA MANE Select	NP_002078.1:p.Gly384=