Canonical Allele Identifier: CA2261354347

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351815A= , CM000679.2:g.44351815A=	GRCh38
NC_000017.10:g.42429183A= , CM000679.1:g.42429183A=	GRCh37
NC_000017.9:g.39784709A=	NCBI36
NG_007886.1:g.11693A= , LRG_661:g.11693A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+20A= MANE Select	ENSP00000053867.2:n.1179+20A=
ENST00000639447.1:c.1136+63A=	ENSP00000492014.1:n.1136+63A=
ENST00000053867.7:c.1179+20A=	ENSP00000053867.2:n.1179+20A=
ENST00000586443.1:c.620+20A=
ENST00000589265.5:c.708+20A=	ENSP00000467616.1:n.708+20A=
NM_002087.3:c.1179+20A=	NP_002078.1:n.1179+20A=
XM_005257253.1:c.1179+20A=	XP_005257310.1:n.1179+20A=
XM_024450730.1:c.1179+20A=	XP_024306498.1:n.1179+20A=
NM_002087.4:c.1179+20A= MANE Select	NP_002078.1:n.1179+20A=