Canonical Allele Identifier: CA399768454
Gene: GRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44352072G>C , CM000679.2:g.44352072G>C GRCh38
NC_000017.10:g.42429440G>C , CM000679.1:g.42429440G>C GRCh37
NC_000017.9:g.39784966G>C NCBI36
NG_007886.1:g.11950G>C , LRG_661:g.11950G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1237G>C MANE Select ENSP00000053867.2:p.Glu413Gln
ENST00000639447.1:c.1136+320G>C ENSP00000492014.1:n.1136+320G>C
ENST00000053867.7:c.1237G>C ENSP00000053867.2:p.Glu413Gln
ENST00000586443.1:c.678G>C
ENST00000589265.5:c.766G>C ENSP00000467616.1:p.Glu256Gln
NM_002087.3:c.1237G>C NP_002078.1:p.Glu413Gln
XM_005257253.1:c.1237G>C XP_005257310.1:p.Glu413Gln
XM_024450730.1:c.1237G>C XP_024306498.1:p.Glu413Gln
NM_002087.4:c.1237G>C MANE Select NP_002078.1:p.Glu413Gln