Canonical Allele Identifier: CA2638210916

Gene: GRN

Linked Data

• gnomAD v4: 17-44352329-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352329C>A , CM000679.2:g.44352329C>A	GRCh38
NC_000017.10:g.42429697C>A , CM000679.1:g.42429697C>A	GRCh37
NC_000017.9:g.39785223C>A	NCBI36
NG_007886.1:g.12207C>A , LRG_661:g.12207C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1414-12C>A MANE Select	ENSP00000053867.2:n.1414-12C>A
ENST00000639447.1:c.1137-200C>A	ENSP00000492014.1:n.1137-200C>A
ENST00000053867.7:c.1414-12C>A	ENSP00000053867.2:n.1414-12C>A
ENST00000586242.1:c.48-12C>A
ENST00000586443.1:c.855-12C>A
ENST00000589265.5:c.943-12C>A	ENSP00000467616.1:n.943-12C>A
NM_002087.3:c.1414-12C>A	NP_002078.1:n.1414-12C>A
XM_005257253.1:c.1414-12C>A	XP_005257310.1:n.1414-12C>A
XM_024450730.1:c.1414-12C>A	XP_024306498.1:n.1414-12C>A
NM_002087.4:c.1414-12C>A MANE Select	NP_002078.1:n.1414-12C>A