Canonical Allele Identifier: CA2261354392

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351908C= , CM000679.2:g.44351908C=	GRCh38
NC_000017.10:g.42429276C= , CM000679.1:g.42429276C=	GRCh37
NC_000017.9:g.39784802C=	NCBI36
NG_007886.1:g.11786C= , LRG_661:g.11786C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1180-107C= MANE Select	ENSP00000053867.2:n.1180-107C=
ENST00000639447.1:c.1136+156C=	ENSP00000492014.1:n.1136+156C=
ENST00000053867.7:c.1180-107C=	ENSP00000053867.2:n.1180-107C=
ENST00000586443.1:c.621-107C=
ENST00000589265.5:c.709-107C=	ENSP00000467616.1:n.709-107C=
NM_002087.3:c.1180-107C=	NP_002078.1:n.1180-107C=
XM_005257253.1:c.1180-107C=	XP_005257310.1:n.1180-107C=
XM_024450730.1:c.1180-107C=	XP_024306498.1:n.1180-107C=
NM_002087.4:c.1180-107C= MANE Select	NP_002078.1:n.1180-107C=