Canonical Allele Identifier: CA290925574
Gene: GRN HGNC NCBI

Linked Data

ClinVar Variation Id: 803426
dbSNP Id: rs34424835

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44350178_44350181dup , CM000679.2:g.44350178_44350181dup GRCh38
NC_000017.10:g.42427546_42427549dup , CM000679.1:g.42427546_42427549dup GRCh37
NC_000017.9:g.39783072_39783075dup NCBI36
NG_007886.1:g.10056_10059dup , LRG_661:g.10056_10059dup

Transcript Alleles

HGVS Amino-acid change
ENST00000053867.8:c.350-50_350-47dup MANE Select ENSP00000053867.2:n.350-50_350-47dup
ENST00000639447.1:c.350-50_350-47dup ENSP00000492014.1:n.350-50_350-47dup
ENST00000053867.7:c.350-50_350-47dup ENSP00000053867.2:n.350-50_350-47dup
ENST00000586782.5:c.350-50_350-47dup ENSP00000468318.1:n.350-50_350-47dup
ENST00000587387.5:c.392-50_392-47dup ENSP00000467431.1:n.392-50_392-47dup
ENST00000587518.5:c.350-50_350-47dup ENSP00000465518.1:n.350-50_350-47dup
ENST00000588143.5:c.350-50_350-47dup ENSP00000465375.1:n.350-50_350-47dup
ENST00000588237.5:c.265-264_265-261dup ENSP00000466611.1:n.265-264_265-261dup
ENST00000589265.5:c.350-50_350-47dup ENSP00000467616.1:n.350-50_350-47dup
ENST00000591740.5:c.350-50_350-47dup ENSP00000467022.1:n.350-50_350-47dup
ENST00000592783.5:c.350-50_350-47dup ENSP00000467870.1:n.350-50_350-47dup
ENST00000593167.5:c.350-50_350-47dup ENSP00000466405.1:n.350-50_350-47dup
NM_002087.3:c.350-50_350-47dup NP_002078.1:n.350-50_350-47dup
XM_005257253.1:c.350-50_350-47dup XP_005257310.1:n.350-50_350-47dup
XM_024450730.1:c.350-50_350-47dup XP_024306498.1:n.350-50_350-47dup
NM_002087.4:c.350-50_350-47dup MANE Select NP_002078.1:n.350-50_350-47dup