Canonical Allele Identifier: CA2261354289

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351716A= , CM000679.2:g.44351716A=	GRCh38
NC_000017.10:g.42429084A= , CM000679.1:g.42429084A=	GRCh37
NC_000017.9:g.39784610A=	NCBI36
NG_007886.1:g.11594A= , LRG_661:g.11594A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1100A= MANE Select	ENSP00000053867.2:p.Asp367=
ENST00000639447.1:c.1100A=	ENSP00000492014.1:p.Asp367=
ENST00000053867.7:c.1100A=	ENSP00000053867.2:p.Asp367=
ENST00000586443.1:c.541A=
ENST00000589265.5:c.629A=	ENSP00000467616.1:p.Asp210=
ENST00000589923.1:n.358A=
NM_002087.3:c.1100A=	NP_002078.1:p.Asp367=
XM_005257253.1:c.1100A=	XP_005257310.1:p.Asp367=
XM_024450730.1:c.1100A=	XP_024306498.1:p.Asp367=
NM_002087.4:c.1100A= MANE Select	NP_002078.1:p.Asp367=