Canonical Allele Identifier: CA2638210792

Gene: GRN

Linked Data

• gnomAD v4: 17-44352288-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352288G>C , CM000679.2:g.44352288G>C	GRCh38
NC_000017.10:g.42429656G>C , CM000679.1:g.42429656G>C	GRCh37
NC_000017.9:g.39785182G>C	NCBI36
NG_007886.1:g.12166G>C , LRG_661:g.12166G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1413+40G>C MANE Select	ENSP00000053867.2:n.1413+40G>C
ENST00000639447.1:c.1137-241G>C	ENSP00000492014.1:n.1137-241G>C
ENST00000053867.7:c.1413+40G>C	ENSP00000053867.2:n.1413+40G>C
ENST00000586242.1:c.47+40G>C
ENST00000586443.1:c.854+40G>C
ENST00000589265.5:c.942+40G>C	ENSP00000467616.1:n.942+40G>C
NM_002087.3:c.1413+40G>C	NP_002078.1:n.1413+40G>C
XM_005257253.1:c.1413+40G>C	XP_005257310.1:n.1413+40G>C
XM_024450730.1:c.1413+40G>C	XP_024306498.1:n.1413+40G>C
NM_002087.4:c.1413+40G>C MANE Select	NP_002078.1:n.1413+40G>C