Canonical Allele Identifier: CA2261354576

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352270C= , CM000679.2:g.44352270C=	GRCh38
NC_000017.10:g.42429638C= , CM000679.1:g.42429638C=	GRCh37
NC_000017.9:g.39785164C=	NCBI36
NG_007886.1:g.12148C= , LRG_661:g.12148C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1413+22C= MANE Select	ENSP00000053867.2:n.1413+22C=
ENST00000639447.1:c.1137-259C=	ENSP00000492014.1:n.1137-259C=
ENST00000053867.7:c.1413+22C=	ENSP00000053867.2:n.1413+22C=
ENST00000586242.1:c.47+22C=
ENST00000586443.1:c.854+22C=
ENST00000589265.5:c.942+22C=	ENSP00000467616.1:n.942+22C=
NM_002087.3:c.1413+22C=	NP_002078.1:n.1413+22C=
XM_005257253.1:c.1413+22C=	XP_005257310.1:n.1413+22C=
XM_024450730.1:c.1413+22C=	XP_024306498.1:n.1413+22C=
NM_002087.4:c.1413+22C= MANE Select	NP_002078.1:n.1413+22C=