Canonical Allele Identifier: CA399768132
Gene: GRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44352027T>A , CM000679.2:g.44352027T>A GRCh38
NC_000017.10:g.42429395T>A , CM000679.1:g.42429395T>A GRCh37
NC_000017.9:g.39784921T>A NCBI36
NG_007886.1:g.11905T>A , LRG_661:g.11905T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1192T>A MANE Select ENSP00000053867.2:p.Ser398Thr
ENST00000639447.1:c.1136+275T>A ENSP00000492014.1:n.1136+275T>A
ENST00000053867.7:c.1192T>A ENSP00000053867.2:p.Ser398Thr
ENST00000586443.1:c.633T>A
ENST00000589265.5:c.721T>A ENSP00000467616.1:p.Ser241Thr
NM_002087.3:c.1192T>A NP_002078.1:p.Ser398Thr
XM_005257253.1:c.1192T>A XP_005257310.1:p.Ser398Thr
XM_024450730.1:c.1192T>A XP_024306498.1:p.Ser398Thr
NM_002087.4:c.1192T>A MANE Select NP_002078.1:p.Ser398Thr