Canonical Allele Identifier: CA2261353823

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44350813C= , CM000679.2:g.44350813C=	GRCh38
NC_000017.10:g.42428181C= , CM000679.1:g.42428181C=	GRCh37
NC_000017.9:g.39783707C=	NCBI36
NG_007886.1:g.10691C= , LRG_661:g.10691C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.708+13C= MANE Select	ENSP00000053867.2:n.708+13C=
ENST00000639447.1:c.708+13C=	ENSP00000492014.1:n.708+13C=
ENST00000053867.7:c.708+13C=	ENSP00000053867.2:n.708+13C=
ENST00000586443.1:c.149+13C=
ENST00000586782.5:c.*118+13C=	ENSP00000468318.1:n.*118+13C=
ENST00000588237.5:c.510+13C=	ENSP00000466611.1:n.510+13C=
ENST00000589265.5:c.462+473C=	ENSP00000467616.1:n.462+473C=
ENST00000589923.1:n.29+13C=
ENST00000590984.1:n.298+13C=
NM_002087.3:c.708+13C=	NP_002078.1:n.708+13C=
XM_005257253.1:c.708+13C=	XP_005257310.1:n.708+13C=
XM_024450730.1:c.708+13C=	XP_024306498.1:n.708+13C=
NM_002087.4:c.708+13C= MANE Select	NP_002078.1:n.708+13C=