Canonical Allele Identifier: CA2261354557

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352218T= , CM000679.2:g.44352218T=	GRCh38
NC_000017.10:g.42429586T= , CM000679.1:g.42429586T=	GRCh37
NC_000017.9:g.39785112T=	NCBI36
NG_007886.1:g.12096T= , LRG_661:g.12096T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1383T= MANE Select	ENSP00000053867.2:p.Gly461=
ENST00000639447.1:c.1137-311T=	ENSP00000492014.1:n.1137-311T=
ENST00000053867.7:c.1383T=	ENSP00000053867.2:p.Gly461=
ENST00000586242.1:c.17T=
ENST00000586443.1:c.824T=
ENST00000589265.5:c.912T=	ENSP00000467616.1:p.Gly304=
NM_002087.3:c.1383T=	NP_002078.1:p.Gly461=
XM_005257253.1:c.1383T=	XP_005257310.1:p.Gly461=
XM_024450730.1:c.1383T=	XP_024306498.1:p.Gly461=
NM_002087.4:c.1383T= MANE Select	NP_002078.1:p.Gly461=