Canonical Allele Identifier: CA225209
Gene: GRN HGNC NCBI

Linked Data

ClinVar Variation Id: 98124
dbSNP Id: rs63751074

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44349266C>T , CM000679.2:g.44349266C>T GRCh38
NC_000017.10:g.42426634C>T , CM000679.1:g.42426634C>T GRCh37
NC_000017.9:g.39782160C>T NCBI36
NG_007886.1:g.9144C>T , LRG_661:g.9144C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.102C>T MANE Select ENSP00000053867.2:p.Pro34=
ENST00000639447.1:c.102C>T ENSP00000492014.1:p.Pro34=
ENST00000053867.7:c.102C>T ENSP00000053867.2:p.Pro34=
ENST00000585512.5:c.102C>T ENSP00000467745.1:p.Pro34=
ENST00000586782.5:c.102C>T ENSP00000468318.1:p.Pro34=
ENST00000587109.5:c.102C>T ENSP00000466271.1:p.Pro34=
ENST00000587387.5:c.102C>T ENSP00000467431.1:p.Pro34=
ENST00000587518.5:c.102C>T ENSP00000465518.1:p.Pro34=
ENST00000587958.1:n.138C>T
ENST00000588143.5:c.102C>T ENSP00000465375.1:p.Pro34=
ENST00000588170.5:n.198C>T
ENST00000588237.5:c.102C>T ENSP00000466611.1:p.Pro34=
ENST00000589265.5:c.102C>T ENSP00000467616.1:p.Pro34=
ENST00000589536.5:c.102C>T ENSP00000466956.1:p.Pro34=
ENST00000591740.5:c.102C>T ENSP00000467022.1:p.Pro34=
ENST00000592323.5:n.142C>T
ENST00000592783.5:c.102C>T ENSP00000467870.1:p.Pro34=
ENST00000593167.5:c.102C>T ENSP00000466405.1:p.Pro34=
NM_002087.3:c.102C>T NP_002078.1:p.Pro34=
XM_005257253.1:c.102C>T XP_005257310.1:p.Pro34=
XM_024450730.1:c.102C>T XP_024306498.1:p.Pro34=
NM_002087.4:c.102C>T MANE Select NP_002078.1:p.Pro34=