Canonical Allele Identifier: CA2261353955

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351044G= , CM000679.2:g.44351044G=	GRCh38
NC_000017.10:g.42428412G= , CM000679.1:g.42428412G=	GRCh37
NC_000017.9:g.39783938G=	NCBI36
NG_007886.1:g.10922G= , LRG_661:g.10922G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.716G= MANE Select	ENSP00000053867.2:p.Cys239=
ENST00000639447.1:c.716G=	ENSP00000492014.1:p.Cys239=
ENST00000053867.7:c.716G=	ENSP00000053867.2:p.Cys239=
ENST00000585348.1:n.134G=
ENST00000586443.1:c.157G=
ENST00000586782.5:c.*126G=	ENSP00000468318.1:n.*126G=
ENST00000588237.5:c.518G=
ENST00000589265.5:c.463-506G=	ENSP00000467616.1:n.463-506G=
ENST00000589923.1:n.37G=
ENST00000590984.1:n.306G=
NM_002087.3:c.716G=	NP_002078.1:p.Cys239=
XM_005257253.1:c.716G=	XP_005257310.1:p.Cys239=
XM_024450730.1:c.716G=	XP_024306498.1:p.Cys239=
NM_002087.4:c.716G= MANE Select	NP_002078.1:p.Cys239=