Canonical Allele Identifier: CA2638207751

Gene: GRN

Linked Data

• gnomAD v4: 17-44350176-G-GAGAC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44350178_44350179insACAG , CM000679.2:g.44350178_44350179insACAG	GRCh38
NC_000017.10:g.42427546_42427547insACAG , CM000679.1:g.42427546_42427547insACAG	GRCh37
NC_000017.9:g.39783072_39783073insACAG	NCBI36
NG_007886.1:g.10056_10057insACAG , LRG_661:g.10056_10057insACAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.350-50_350-49insACAG MANE Select	ENSP00000053867.2:n.350-50_350-49insACAG
ENST00000639447.1:c.350-50_350-49insACAG	ENSP00000492014.1:n.350-50_350-49insACAG
ENST00000053867.7:c.350-50_350-49insACAG	ENSP00000053867.2:n.350-50_350-49insACAG
ENST00000586782.5:c.350-50_350-49insACAG	ENSP00000468318.1:n.350-50_350-49insACAG
ENST00000587387.5:c.392-50_392-49insACAG	ENSP00000467431.1:n.392-50_392-49insACAG
ENST00000587518.5:c.350-50_350-49insACAG	ENSP00000465518.1:n.350-50_350-49insACAG
ENST00000588143.5:c.350-50_350-49insACAG	ENSP00000465375.1:n.350-50_350-49insACAG
ENST00000588237.5:c.265-264_265-263insACAG	ENSP00000466611.1:n.265-264_265-263insACAG
ENST00000589265.5:c.350-50_350-49insACAG	ENSP00000467616.1:n.350-50_350-49insACAG
ENST00000591740.5:c.350-50_350-49insACAG	ENSP00000467022.1:n.350-50_350-49insACAG
ENST00000592783.5:c.350-50_350-49insACAG	ENSP00000467870.1:n.350-50_350-49insACAG
ENST00000593167.5:c.350-50_350-49insACAG	ENSP00000466405.1:n.350-50_350-49insACAG
NM_002087.3:c.350-50_350-49insACAG	NP_002078.1:n.350-50_350-49insACAG
XM_005257253.1:c.350-50_350-49insACAG	XP_005257310.1:n.350-50_350-49insACAG
XM_024450730.1:c.350-50_350-49insACAG	XP_024306498.1:n.350-50_350-49insACAG
NM_002087.4:c.350-50_350-49insACAG MANE Select	NP_002078.1:n.350-50_350-49insACAG