Canonical Allele Identifier: CA2261354493

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352090G= , CM000679.2:g.44352090G=	GRCh38
NC_000017.10:g.42429458G= , CM000679.1:g.42429458G=	GRCh37
NC_000017.9:g.39784984G=	NCBI36
NG_007886.1:g.11968G= , LRG_661:g.11968G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1255G= MANE Select	ENSP00000053867.2:p.Gly419=
ENST00000639447.1:c.1136+338G=	ENSP00000492014.1:n.1136+338G=
ENST00000053867.7:c.1255G=	ENSP00000053867.2:p.Gly419=
ENST00000586443.1:c.696G=
ENST00000589265.5:c.784G=	ENSP00000467616.1:p.Gly262=
NM_002087.3:c.1255G=	NP_002078.1:p.Gly419=
XM_005257253.1:c.1255G=	XP_005257310.1:p.Gly419=
XM_024450730.1:c.1255G=	XP_024306498.1:p.Gly419=
NM_002087.4:c.1255G= MANE Select	NP_002078.1:p.Gly419=