Canonical Allele Identifier: CA2261354601

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352313T= , CM000679.2:g.44352313T=	GRCh38
NC_000017.10:g.42429681T= , CM000679.1:g.42429681T=	GRCh37
NC_000017.9:g.39785207T=	NCBI36
NG_007886.1:g.12191T= , LRG_661:g.12191T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1414-28T= MANE Select	ENSP00000053867.2:n.1414-28T=
ENST00000639447.1:c.1137-216T=	ENSP00000492014.1:n.1137-216T=
ENST00000053867.7:c.1414-28T=	ENSP00000053867.2:n.1414-28T=
ENST00000586242.1:c.48-28T=
ENST00000586443.1:c.855-28T=
ENST00000589265.5:c.943-28T=	ENSP00000467616.1:n.943-28T=
NM_002087.3:c.1414-28T=	NP_002078.1:n.1414-28T=
XM_005257253.1:c.1414-28T=	XP_005257310.1:n.1414-28T=
XM_024450730.1:c.1414-28T=	XP_024306498.1:n.1414-28T=
NM_002087.4:c.1414-28T= MANE Select	NP_002078.1:n.1414-28T=