Canonical Allele Identifier: CA399766128
Gene: GRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42429104T>A (hg19) chr17:g.44351736T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44351736T>A , CM000679.2:g.44351736T>A GRCh38
NC_000017.10:g.42429104T>A , CM000679.1:g.42429104T>A GRCh37
NC_000017.9:g.39784630T>A NCBI36
NG_007886.1:g.11614T>A , LRG_661:g.11614T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1120T>A MANE Select ENSP00000053867.2:p.Ser374Thr
ENST00000639447.1:c.1120T>A ENSP00000492014.1:p.Ser374Thr
ENST00000053867.7:c.1120T>A ENSP00000053867.2:p.Ser374Thr
ENST00000586443.1:c.561T>A
ENST00000589265.5:c.649T>A ENSP00000467616.1:p.Ser217Thr
ENST00000589923.1:n.378T>A
NM_002087.3:c.1120T>A NP_002078.1:p.Ser374Thr
XM_005257253.1:c.1120T>A XP_005257310.1:p.Ser374Thr
XM_024450730.1:c.1120T>A XP_024306498.1:p.Ser374Thr
NM_002087.4:c.1120T>A MANE Select NP_002078.1:p.Ser374Thr
Search 100 bp 5'
Search 100 bp 3'