Canonical Allele Identifier: CA2261353560

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44350341G= , CM000679.2:g.44350341G=	GRCh38
NC_000017.10:g.42427709G= , CM000679.1:g.42427709G=	GRCh37
NC_000017.9:g.39783235G=	NCBI36
NG_007886.1:g.10219G= , LRG_661:g.10219G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002087.4:c.462+1G= MANE Select	NP_002078.1:n.462+1G=
ENST00000053867.8:c.462+1G= MANE Select	ENSP00000053867.2:n.462+1G=
NM_002087.3:c.462+1G=	NP_002078.1:n.462+1G=
ENST00000053867.7:c.462+1G=	ENSP00000053867.2:n.462+1G=
ENST00000586782.5:c.462+1G=	ENSP00000468318.1:n.462+1G=
ENST00000587387.5:c.504+1G=	ENSP00000467431.1:n.504+1G=
ENST00000588143.5:c.462+1G=	ENSP00000465375.1:n.462+1G=
ENST00000588237.5:c.265-101G=	ENSP00000466611.1:n.265-101G=
ENST00000589265.5:c.462+1G=	ENSP00000467616.1:n.462+1G=
ENST00000590984.1:n.52+1G=
ENST00000639447.1:c.462+1G=	ENSP00000492014.1:n.462+1G=
XM_005257253.1:c.462+1G=	XP_005257310.1:n.462+1G=
XM_024450730.1:c.462+1G=	XP_024306498.1:n.462+1G=