Canonical Allele Identifier: CA8601794

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44349515C>T , CM000679.2:g.44349515C>T	GRCh38
NC_000017.10:g.42426883C>T , CM000679.1:g.42426883C>T	GRCh37
NC_000017.9:g.39782409C>T	NCBI36
NG_007886.1:g.9393C>T , LRG_661:g.9393C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002087.4:c.228C>T MANE Select	NP_002078.1:p.Thr76=
ENST00000053867.8:c.228C>T MANE Select	ENSP00000053867.2:p.Thr76=
NM_002087.3:c.228C>T	NP_002078.1:p.Thr76=
ENST00000053867.7:c.228C>T	ENSP00000053867.2:p.Thr76=
ENST00000586782.5:c.228C>T	ENSP00000468318.1:p.Thr76=
ENST00000587387.5:c.228C>T	ENSP00000467431.1:p.Thr76=
ENST00000587518.5:c.228C>T	ENSP00000465518.1:p.Thr76=
ENST00000587958.1:n.264C>T
ENST00000588143.5:c.228C>T	ENSP00000465375.1:p.Thr76=
ENST00000588170.5:n.324C>T
ENST00000588237.5:c.228C>T	ENSP00000466611.1:p.Thr76=
ENST00000589265.5:c.228C>T	ENSP00000467616.1:p.Thr76=
ENST00000589536.5:c.228C>T	ENSP00000466956.1:p.Thr76=
ENST00000591740.5:c.228C>T	ENSP00000467022.1:p.Thr76=
ENST00000592323.5:n.391C>T
ENST00000592783.5:c.228C>T	ENSP00000467870.1:p.Thr76=
ENST00000593167.5:c.228C>T	ENSP00000466405.1:p.Thr76=
ENST00000639447.1:c.228C>T	ENSP00000492014.1:p.Thr76=
XM_005257253.1:c.228C>T	XP_005257310.1:p.Thr76=
XM_024450730.1:c.228C>T	XP_024306498.1:p.Thr76=