Canonical Allele Identifier: CA399759637
Gene: GRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44349447A>G , CM000679.2:g.44349447A>G GRCh38
NC_000017.10:g.42426815A>G , CM000679.1:g.42426815A>G GRCh37
NC_000017.9:g.39782341A>G NCBI36
NG_007886.1:g.9325A>G , LRG_661:g.9325A>G

Transcript Alleles

HGVS Amino-acid Change
NM_002087.4:c.160A>G MANE Select NP_002078.1:p.Ser54Gly
ENST00000053867.8:c.160A>G MANE Select ENSP00000053867.2:p.Ser54Gly
NM_002087.3:c.160A>G NP_002078.1:p.Ser54Gly
ENST00000053867.7:c.160A>G ENSP00000053867.2:p.Ser54Gly
ENST00000586782.5:c.160A>G ENSP00000468318.1:p.Ser54Gly
ENST00000587109.5:c.160A>G ENSP00000466271.1:p.Ser54Gly
ENST00000587387.5:c.160A>G ENSP00000467431.1:p.Ser54Gly
ENST00000587518.5:c.160A>G ENSP00000465518.1:p.Ser54Gly
ENST00000587958.1:n.196A>G
ENST00000588143.5:c.160A>G ENSP00000465375.1:p.Ser54Gly
ENST00000588170.5:n.256A>G
ENST00000588237.5:c.160A>G ENSP00000466611.1:p.Ser54Gly
ENST00000589265.5:c.160A>G ENSP00000467616.1:p.Ser54Gly
ENST00000589536.5:c.160A>G ENSP00000466956.1:p.Ser54Gly
ENST00000591740.5:c.160A>G ENSP00000467022.1:p.Ser54Gly
ENST00000592323.5:n.323A>G
ENST00000592783.5:c.160A>G ENSP00000467870.1:p.Ser54Gly
ENST00000593167.5:c.160A>G ENSP00000466405.1:p.Ser54Gly
ENST00000639447.1:c.160A>G ENSP00000492014.1:p.Ser54Gly
XM_005257253.1:c.160A>G XP_005257310.1:p.Ser54Gly
XM_024450730.1:c.160A>G XP_024306498.1:p.Ser54Gly