Canonical Allele Identifier: CA2809588855

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351851_44351852insACA , CM000679.2:g.44351851_44351852insACA	GRCh38
NC_000017.10:g.42429219_42429220insACA , CM000679.1:g.42429219_42429220insACA	GRCh37
NC_000017.9:g.39784745_39784746insACA	NCBI36
NG_007886.1:g.11729_11730insACA , LRG_661:g.11729_11730insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+56_1179+57insACA MANE Select	ENSP00000053867.2:n.1179+56_1179+57insACA
ENST00000639447.1:c.1136+99_1136+100insACA	ENSP00000492014.1:n.1136+99_1136+100insACA
ENST00000053867.7:c.1179+56_1179+57insACA	ENSP00000053867.2:n.1179+56_1179+57insACA
ENST00000586443.1:c.620+56_620+57insACA
ENST00000589265.5:c.708+56_708+57insACA	ENSP00000467616.1:n.708+56_708+57insACA
NM_002087.3:c.1179+56_1179+57insACA	NP_002078.1:n.1179+56_1179+57insACA
XM_005257253.1:c.1179+56_1179+57insACA	XP_005257310.1:n.1179+56_1179+57insACA
XM_024450730.1:c.1179+56_1179+57insACA	XP_024306498.1:n.1179+56_1179+57insACA
NM_002087.4:c.1179+56_1179+57insACA MANE Select	NP_002078.1:n.1179+56_1179+57insACA