Canonical Allele Identifier: CA2261354528

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352166G= , CM000679.2:g.44352166G=	GRCh38
NC_000017.10:g.42429534G= , CM000679.1:g.42429534G=	GRCh37
NC_000017.9:g.39785060G=	NCBI36
NG_007886.1:g.12044G= , LRG_661:g.12044G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1331G= MANE Select	ENSP00000053867.2:p.Cys444=
ENST00000639447.1:c.1137-363G=	ENSP00000492014.1:n.1137-363G=
ENST00000053867.7:c.1331G=	ENSP00000053867.2:p.Cys444=
ENST00000586443.1:c.772G=
ENST00000589265.5:c.860G=	ENSP00000467616.1:p.Cys287=
NM_002087.3:c.1331G=	NP_002078.1:p.Cys444=
XM_005257253.1:c.1331G=	XP_005257310.1:p.Cys444=
XM_024450730.1:c.1331G=	XP_024306498.1:p.Cys444=
NM_002087.4:c.1331G= MANE Select	NP_002078.1:p.Cys444=