Canonical Allele Identifier: CA399764797

Gene: GRN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351164G>C , CM000679.2:g.44351164G>C	GRCh38
NC_000017.10:g.42428532G>C , CM000679.1:g.42428532G>C	GRCh37
NC_000017.9:g.39784058G>C	NCBI36
NG_007886.1:g.11042G>C , LRG_661:g.11042G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.835+1G>C MANE Select	ENSP00000053867.2:n.835+1G>C
ENST00000639447.1:c.835+1G>C	ENSP00000492014.1:n.835+1G>C
ENST00000053867.7:c.835+1G>C	ENSP00000053867.2:n.835+1G>C
ENST00000585348.1:n.254G>C
ENST00000586443.1:c.276+1G>C
ENST00000589265.5:c.463-386G>C	ENSP00000467616.1:n.463-386G>C
ENST00000589923.1:n.93+64G>C
ENST00000590984.1:n.426G>C
NM_002087.3:c.835+1G>C	NP_002078.1:n.835+1G>C
XM_005257253.1:c.835+1G>C	XP_005257310.1:n.835+1G>C
XM_024450730.1:c.835+1G>C	XP_024306498.1:n.835+1G>C
NM_002087.4:c.835+1G>C MANE Select	NP_002078.1:n.835+1G>C