Canonical Allele Identifier: CA2261354360

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351837G= , CM000679.2:g.44351837G=	GRCh38
NC_000017.10:g.42429205G= , CM000679.1:g.42429205G=	GRCh37
NC_000017.9:g.39784731G=	NCBI36
NG_007886.1:g.11715G= , LRG_661:g.11715G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+42G= MANE Select	ENSP00000053867.2:n.1179+42G=
ENST00000639447.1:c.1136+85G=	ENSP00000492014.1:n.1136+85G=
ENST00000053867.7:c.1179+42G=	ENSP00000053867.2:n.1179+42G=
ENST00000586443.1:c.620+42G=
ENST00000589265.5:c.708+42G=	ENSP00000467616.1:n.708+42G=
NM_002087.3:c.1179+42G=	NP_002078.1:n.1179+42G=
XM_005257253.1:c.1179+42G=	XP_005257310.1:n.1179+42G=
XM_024450730.1:c.1179+42G=	XP_024306498.1:n.1179+42G=
NM_002087.4:c.1179+42G= MANE Select	NP_002078.1:n.1179+42G=