Canonical Allele Identifier: CA8601790
Gene: GRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44349495G>A , CM000679.2:g.44349495G>A GRCh38
NC_000017.10:g.42426863G>A , CM000679.1:g.42426863G>A GRCh37
NC_000017.9:g.39782389G>A NCBI36
NG_007886.1:g.9373G>A , LRG_661:g.9373G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.208G>A MANE Select ENSP00000053867.2:p.Gly70Ser
ENST00000639447.1:c.208G>A ENSP00000492014.1:p.Gly70Ser
ENST00000053867.7:c.208G>A ENSP00000053867.2:p.Gly70Ser
ENST00000586782.5:c.208G>A ENSP00000468318.1:p.Gly70Ser
ENST00000587387.5:c.208G>A ENSP00000467431.1:p.Gly70Ser
ENST00000587518.5:c.208G>A ENSP00000465518.1:p.Gly70Ser
ENST00000587958.1:n.244G>A
ENST00000588143.5:c.208G>A ENSP00000465375.1:p.Gly70Ser
ENST00000588170.5:n.304G>A
ENST00000588237.5:c.208G>A ENSP00000466611.1:p.Gly70Ser
ENST00000589265.5:c.208G>A ENSP00000467616.1:p.Gly70Ser
ENST00000589536.5:c.208G>A ENSP00000466956.1:p.Gly70Ser
ENST00000591740.5:c.208G>A ENSP00000467022.1:p.Gly70Ser
ENST00000592323.5:n.371G>A
ENST00000592783.5:c.208G>A ENSP00000467870.1:p.Gly70Ser
ENST00000593167.5:c.208G>A ENSP00000466405.1:p.Gly70Ser
NM_002087.3:c.208G>A NP_002078.1:p.Gly70Ser
XM_005257253.1:c.208G>A XP_005257310.1:p.Gly70Ser
XM_024450730.1:c.208G>A XP_024306498.1:p.Gly70Ser
NM_002087.4:c.208G>A MANE Select NP_002078.1:p.Gly70Ser