Canonical Allele Identifier: CA2261354257

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351649A= , CM000679.2:g.44351649A=	GRCh38
NC_000017.10:g.42429017A= , CM000679.1:g.42429017A=	GRCh37
NC_000017.9:g.39784543A=	NCBI36
NG_007886.1:g.11527A= , LRG_661:g.11527A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1033A= MANE Select	ENSP00000053867.2:p.Met345=
ENST00000639447.1:c.1033A=	ENSP00000492014.1:p.Met345=
ENST00000053867.7:c.1033A=	ENSP00000053867.2:p.Met345=
ENST00000586443.1:c.474A=
ENST00000589265.5:c.562A=	ENSP00000467616.1:p.Met188=
ENST00000589923.1:n.291A=
NM_002087.3:c.1033A=	NP_002078.1:p.Met345=
XM_005257253.1:c.1033A=	XP_005257310.1:p.Met345=
XM_024450730.1:c.1033A=	XP_024306498.1:p.Met345=
NM_002087.4:c.1033A= MANE Select	NP_002078.1:p.Met345=