Canonical Allele Identifier: CA2261353175
Gene: GRN HGNC NCBI

Linked Data

dbSNP Id: rs2048352542

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44349573T>C , CM000679.2:g.44349573T>C GRCh38
NC_000017.10:g.42426941T>C , CM000679.1:g.42426941T>C GRCh37
NC_000017.9:g.39782467T>C NCBI36
NG_007886.1:g.9451T>C , LRG_661:g.9451T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000053867.8:c.264+22T>C MANE Select ENSP00000053867.2:n.264+22T>C
ENST00000639447.1:c.264+22T>C ENSP00000492014.1:n.264+22T>C
ENST00000053867.7:c.264+22T>C ENSP00000053867.2:n.264+22T>C
ENST00000586782.5:c.264+22T>C ENSP00000468318.1:n.264+22T>C
ENST00000587387.5:c.264+22T>C ENSP00000467431.1:n.264+22T>C
ENST00000587518.5:c.264+22T>C ENSP00000465518.1:n.264+22T>C
ENST00000587958.1:n.322T>C
ENST00000588143.5:c.264+22T>C ENSP00000465375.1:n.264+22T>C
ENST00000588170.5:n.360+22T>C
ENST00000588237.5:c.264+22T>C ENSP00000466611.1:n.264+22T>C
ENST00000589265.5:c.264+22T>C ENSP00000467616.1:n.264+22T>C
ENST00000589536.5:c.264+22T>C ENSP00000466956.1:n.264+22T>C
ENST00000591740.5:c.264+22T>C ENSP00000467022.1:n.264+22T>C
ENST00000592323.5:n.427+22T>C
ENST00000592783.5:c.264+22T>C ENSP00000467870.1:n.264+22T>C
ENST00000593167.5:c.264+22T>C ENSP00000466405.1:n.264+22T>C
NM_002087.3:c.264+22T>C NP_002078.1:n.264+22T>C
XM_005257253.1:c.264+22T>C XP_005257310.1:n.264+22T>C
XM_024450730.1:c.264+22T>C XP_024306498.1:n.264+22T>C
NM_002087.4:c.264+22T>C MANE Select NP_002078.1:n.264+22T>C