Canonical Allele Identifier: CA2261354288
Gene: GRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44351715_44351718delinsGATA , CM000679.2:g.44351715_44351718delinsGATA GRCh38
NC_000017.10:g.42429083_42429086delinsGATA , CM000679.1:g.42429083_42429086delinsGATA GRCh37
NC_000017.9:g.39784609_39784612delinsGATA NCBI36
NG_007886.1:g.11593_11596delinsGATA , LRG_661:g.11593_11596delinsGATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1099_1102delinsGATA MANE Select ENSP00000053867.2:p.Asp367=
ENST00000639447.1:c.1099_1102delinsGATA ENSP00000492014.1:p.Asp367=
ENST00000053867.7:c.1099_1102delinsGATA ENSP00000053867.2:p.Asp367=
ENST00000586443.1:c.540_543delinsGATA
ENST00000589265.5:c.628_631delinsGATA ENSP00000467616.1:p.Asp210=
ENST00000589923.1:n.357_360delinsGATA
NM_002087.3:c.1099_1102delinsGATA NP_002078.1:p.Asp367=
XM_005257253.1:c.1099_1102delinsGATA XP_005257310.1:p.Asp367=
XM_024450730.1:c.1099_1102delinsGATA XP_024306498.1:p.Asp367=
NM_002087.4:c.1099_1102delinsGATA MANE Select NP_002078.1:p.Asp367=