Canonical Allele Identifier: CA2261353579

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44350364G= , CM000679.2:g.44350364G=	GRCh38
NC_000017.10:g.42427732G= , CM000679.1:g.42427732G=	GRCh37
NC_000017.9:g.39783258G=	NCBI36
NG_007886.1:g.10242G= , LRG_661:g.10242G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.462+24G= MANE Select	ENSP00000053867.2:n.462+24G=
ENST00000639447.1:c.462+24G=	ENSP00000492014.1:n.462+24G=
ENST00000053867.7:c.462+24G=	ENSP00000053867.2:n.462+24G=
ENST00000586782.5:c.462+24G=	ENSP00000468318.1:n.462+24G=
ENST00000587387.5:c.504+24G=	ENSP00000467431.1:n.504+24G=
ENST00000588143.5:c.462+24G=	ENSP00000465375.1:n.462+24G=
ENST00000588237.5:c.265-78G=	ENSP00000466611.1:n.265-78G=
ENST00000589265.5:c.462+24G=	ENSP00000467616.1:n.462+24G=
ENST00000590984.1:n.52+24G=
NM_002087.3:c.462+24G=	NP_002078.1:n.462+24G=
XM_005257253.1:c.462+24G=	XP_005257310.1:n.462+24G=
XM_024450730.1:c.462+24G=	XP_024306498.1:n.462+24G=
NM_002087.4:c.462+24G= MANE Select	NP_002078.1:n.462+24G=