Canonical Allele Identifier: CA2261354598
Gene: GRN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44352310T= , CM000679.2:g.44352310T= GRCh38
NC_000017.10:g.42429678T= , CM000679.1:g.42429678T= GRCh37
NC_000017.9:g.39785204T= NCBI36
NG_007886.1:g.12188T= , LRG_661:g.12188T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1414-31T= MANE Select ENSP00000053867.2:n.1414-31T=
ENST00000639447.1:c.1137-219T= ENSP00000492014.1:n.1137-219T=
ENST00000053867.7:c.1414-31T= ENSP00000053867.2:n.1414-31T=
ENST00000586242.1:c.48-31T=
ENST00000586443.1:c.855-31T=
ENST00000589265.5:c.943-31T= ENSP00000467616.1:n.943-31T=
NM_002087.3:c.1414-31T= NP_002078.1:n.1414-31T=
XM_005257253.1:c.1414-31T= XP_005257310.1:n.1414-31T=
XM_024450730.1:c.1414-31T= XP_024306498.1:n.1414-31T=
NM_002087.4:c.1414-31T= MANE Select NP_002078.1:n.1414-31T=
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