Canonical Allele Identifier: CA2638210785

Gene: GRN

Linked Data

• gnomAD v4: 17-44352283-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352283G>T , CM000679.2:g.44352283G>T	GRCh38
NC_000017.10:g.42429651G>T , CM000679.1:g.42429651G>T	GRCh37
NC_000017.9:g.39785177G>T	NCBI36
NG_007886.1:g.12161G>T , LRG_661:g.12161G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1413+35G>T MANE Select	ENSP00000053867.2:n.1413+35G>T
ENST00000639447.1:c.1137-246G>T	ENSP00000492014.1:n.1137-246G>T
ENST00000053867.7:c.1413+35G>T	ENSP00000053867.2:n.1413+35G>T
ENST00000586242.1:c.47+35G>T
ENST00000586443.1:c.854+35G>T
ENST00000589265.5:c.942+35G>T	ENSP00000467616.1:n.942+35G>T
NM_002087.3:c.1413+35G>T	NP_002078.1:n.1413+35G>T
XM_005257253.1:c.1413+35G>T	XP_005257310.1:n.1413+35G>T
XM_024450730.1:c.1413+35G>T	XP_024306498.1:n.1413+35G>T
NM_002087.4:c.1413+35G>T MANE Select	NP_002078.1:n.1413+35G>T