Canonical Allele Identifier: CA399768965
Gene: GRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42429528T>G (hg19) chr17:g.44352160T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44352160T>G , CM000679.2:g.44352160T>G GRCh38
NC_000017.10:g.42429528T>G , CM000679.1:g.42429528T>G GRCh37
NC_000017.9:g.39785054T>G NCBI36
NG_007886.1:g.12038T>G , LRG_661:g.12038T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1325T>G MANE Select ENSP00000053867.2:p.Ile442Ser
ENST00000639447.1:c.1137-369T>G ENSP00000492014.1:n.1137-369T>G
ENST00000053867.7:c.1325T>G ENSP00000053867.2:p.Ile442Ser
ENST00000586443.1:c.766T>G
ENST00000589265.5:c.854T>G ENSP00000467616.1:p.Ile285Ser
NM_002087.3:c.1325T>G NP_002078.1:p.Ile442Ser
XM_005257253.1:c.1325T>G XP_005257310.1:p.Ile442Ser
XM_024450730.1:c.1325T>G XP_024306498.1:p.Ile442Ser
NM_002087.4:c.1325T>G MANE Select NP_002078.1:p.Ile442Ser
Search 100 bp 5'
Search 100 bp 3'