Canonical Allele Identifier: CA399766046
Gene: GRN HGNC NCBI

Linked Data

gnomAD v4: 17-44351728-G-A
MyVariant Identifiers: chr17:g.42429096G>A (hg19) chr17:g.44351728G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44351728G>A , CM000679.2:g.44351728G>A GRCh38
NC_000017.10:g.42429096G>A , CM000679.1:g.42429096G>A GRCh37
NC_000017.9:g.39784622G>A NCBI36
NG_007886.1:g.11606G>A , LRG_661:g.11606G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1112G>A MANE Select ENSP00000053867.2:p.Ser371Asn
ENST00000639447.1:c.1112G>A ENSP00000492014.1:p.Ser371Asn
ENST00000053867.7:c.1112G>A ENSP00000053867.2:p.Ser371Asn
ENST00000586443.1:c.553G>A
ENST00000589265.5:c.641G>A ENSP00000467616.1:p.Ser214Asn
ENST00000589923.1:n.370G>A
NM_002087.3:c.1112G>A NP_002078.1:p.Ser371Asn
XM_005257253.1:c.1112G>A XP_005257310.1:p.Ser371Asn
XM_024450730.1:c.1112G>A XP_024306498.1:p.Ser371Asn
NM_002087.4:c.1112G>A MANE Select NP_002078.1:p.Ser371Asn
Search 100 bp 5'
Search 100 bp 3'