Canonical Allele Identifier: CA2261353189

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44349599C= , CM000679.2:g.44349599C=	GRCh38
NC_000017.10:g.42426967C= , CM000679.1:g.42426967C=	GRCh37
NC_000017.9:g.39782493C=	NCBI36
NG_007886.1:g.9477C= , LRG_661:g.9477C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.264+48C= MANE Select	ENSP00000053867.2:n.264+48C=
ENST00000639447.1:c.264+48C=	ENSP00000492014.1:n.264+48C=
ENST00000053867.7:c.264+48C=	ENSP00000053867.2:n.264+48C=
ENST00000586782.5:c.264+48C=	ENSP00000468318.1:n.264+48C=
ENST00000587387.5:c.265-26C=	ENSP00000467431.1:n.265-26C=
ENST00000587518.5:c.264+48C=	ENSP00000465518.1:n.264+48C=
ENST00000587958.1:n.348C=
ENST00000588143.5:c.264+48C=	ENSP00000465375.1:n.264+48C=
ENST00000588170.5:n.360+48C=
ENST00000588237.5:c.264+48C=	ENSP00000466611.1:n.264+48C=
ENST00000589265.5:c.264+48C=	ENSP00000467616.1:n.264+48C=
ENST00000589536.5:c.264+48C=	ENSP00000466956.1:n.264+48C=
ENST00000591740.5:c.264+48C=	ENSP00000467022.1:n.264+48C=
ENST00000592323.5:n.427+48C=
ENST00000592783.5:c.264+48C=	ENSP00000467870.1:n.264+48C=
ENST00000593167.5:c.264+48C=	ENSP00000466405.1:n.264+48C=
NM_002087.3:c.264+48C=	NP_002078.1:n.264+48C=
XM_005257253.1:c.264+48C=	XP_005257310.1:n.264+48C=
XM_024450730.1:c.264+48C=	XP_024306498.1:n.264+48C=
NM_002087.4:c.264+48C= MANE Select	NP_002078.1:n.264+48C=