Canonical Allele Identifier: CA8601820

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44349669C>T , CM000679.2:g.44349669C>T	GRCh38
NC_000017.10:g.42427037C>T , CM000679.1:g.42427037C>T	GRCh37
NC_000017.9:g.39782563C>T	NCBI36
NG_007886.1:g.9547C>T , LRG_661:g.9547C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002087.4:c.267C>T MANE Select	NP_002078.1:p.Ala89=
ENST00000053867.8:c.267C>T MANE Select	ENSP00000053867.2:p.Ala89=
NM_002087.3:c.267C>T	NP_002078.1:p.Ala89=
ENST00000053867.7:c.267C>T	ENSP00000053867.2:p.Ala89=
ENST00000586782.5:c.267C>T	ENSP00000468318.1:p.Ala89=
ENST00000587387.5:c.309C>T	ENSP00000467431.1:p.Ala103=
ENST00000587518.5:c.267C>T	ENSP00000465518.1:p.Ala89=
ENST00000587958.1:n.418C>T
ENST00000588143.5:c.267C>T	ENSP00000465375.1:p.Ala89=
ENST00000588170.5:n.363C>T
ENST00000588237.5:c.264+118C>T	ENSP00000466611.1:n.264+118C>T
ENST00000589265.5:c.267C>T	ENSP00000467616.1:p.Ala89=
ENST00000589536.5:c.267C>T	ENSP00000466956.1:p.Ala89=
ENST00000591740.5:c.267C>T	ENSP00000467022.1:p.Ala89=
ENST00000592323.5:n.430C>T
ENST00000592783.5:c.267C>T	ENSP00000467870.1:p.Ala89=
ENST00000593167.5:c.267C>T	ENSP00000466405.1:p.Ala89=
ENST00000639447.1:c.267C>T	ENSP00000492014.1:p.Ala89=
XM_005257253.1:c.267C>T	XP_005257310.1:p.Ala89=
XM_024450730.1:c.267C>T	XP_024306498.1:p.Ala89=