Canonical Allele Identifier: CA2261354296

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351727_44351729delinsAGC , CM000679.2:g.44351727_44351729delinsAGC	GRCh38
NC_000017.10:g.42429095_42429097delinsAGC , CM000679.1:g.42429095_42429097delinsAGC	GRCh37
NC_000017.9:g.39784621_39784623delinsAGC	NCBI36
NG_007886.1:g.11605_11607delinsAGC , LRG_661:g.11605_11607delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1111_1113delinsAGC MANE Select	ENSP00000053867.2:p.Ser371=
ENST00000639447.1:c.1111_1113delinsAGC	ENSP00000492014.1:p.Ser371=
ENST00000053867.7:c.1111_1113delinsAGC	ENSP00000053867.2:p.Ser371=
ENST00000586443.1:c.552_554delinsAGC
ENST00000589265.5:c.640_642delinsAGC	ENSP00000467616.1:p.Ser214=
ENST00000589923.1:n.369_371delinsAGC
NM_002087.3:c.1111_1113delinsAGC	NP_002078.1:p.Ser371=
XM_005257253.1:c.1111_1113delinsAGC	XP_005257310.1:p.Ser371=
XM_024450730.1:c.1111_1113delinsAGC	XP_024306498.1:p.Ser371=
NM_002087.4:c.1111_1113delinsAGC MANE Select	NP_002078.1:p.Ser371=