Canonical Allele Identifier: CA2261353121

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44349474G= , CM000679.2:g.44349474G=	GRCh38
NC_000017.10:g.42426842G= , CM000679.1:g.42426842G=	GRCh37
NC_000017.9:g.39782368G=	NCBI36
NG_007886.1:g.9352G= , LRG_661:g.9352G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.187G= MANE Select	ENSP00000053867.2:p.Val63=
ENST00000639447.1:c.187G=	ENSP00000492014.1:p.Val63=
ENST00000053867.7:c.187G=	ENSP00000053867.2:p.Val63=
ENST00000586782.5:c.187G=	ENSP00000468318.1:p.Val63=
ENST00000587109.5:c.187G=
ENST00000587387.5:c.187G=	ENSP00000467431.1:p.Val63=
ENST00000587518.5:c.187G=	ENSP00000465518.1:p.Val63=
ENST00000587958.1:n.223G=
ENST00000588143.5:c.187G=	ENSP00000465375.1:p.Val63=
ENST00000588170.5:n.283G=
ENST00000588237.5:c.187G=	ENSP00000466611.1:p.Val63=
ENST00000589265.5:c.187G=	ENSP00000467616.1:p.Val63=
ENST00000589536.5:c.187G=	ENSP00000466956.1:p.Val63=
ENST00000591740.5:c.187G=	ENSP00000467022.1:p.Val63=
ENST00000592323.5:n.350G=
ENST00000592783.5:c.187G=	ENSP00000467870.1:p.Val63=
ENST00000593167.5:c.187G=	ENSP00000466405.1:p.Val63=
NM_002087.3:c.187G=	NP_002078.1:p.Val63=
XM_005257253.1:c.187G=	XP_005257310.1:p.Val63=
XM_024450730.1:c.187G=	XP_024306498.1:p.Val63=
NM_002087.4:c.187G= MANE Select	NP_002078.1:p.Val63=