Canonical Allele Identifier: CA2261353959

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351052G= , CM000679.2:g.44351052G=	GRCh38
NC_000017.10:g.42428420G= , CM000679.1:g.42428420G=	GRCh37
NC_000017.9:g.39783946G=	NCBI36
NG_007886.1:g.10930G= , LRG_661:g.10930G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.724G= MANE Select	ENSP00000053867.2:p.Asp242=
ENST00000639447.1:c.724G=	ENSP00000492014.1:p.Asp242=
ENST00000053867.7:c.724G=	ENSP00000053867.2:p.Asp242=
ENST00000585348.1:n.142G=
ENST00000586443.1:c.165G=
ENST00000586782.5:c.*134G=	ENSP00000468318.1:n.*134G=
ENST00000589265.5:c.463-498G=	ENSP00000467616.1:n.463-498G=
ENST00000589923.1:n.45G=
ENST00000590984.1:n.314G=
NM_002087.3:c.724G=	NP_002078.1:p.Asp242=
XM_005257253.1:c.724G=	XP_005257310.1:p.Asp242=
XM_024450730.1:c.724G=	XP_024306498.1:p.Asp242=
NM_002087.4:c.724G= MANE Select	NP_002078.1:p.Asp242=