Canonical Allele Identifier: CA2261354342
Gene: GRN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44351807G= , CM000679.2:g.44351807G= GRCh38
NC_000017.10:g.42429175G= , CM000679.1:g.42429175G= GRCh37
NC_000017.9:g.39784701G= NCBI36
NG_007886.1:g.11685G= , LRG_661:g.11685G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1179+12G= MANE Select ENSP00000053867.2:n.1179+12G=
ENST00000639447.1:c.1136+55G= ENSP00000492014.1:n.1136+55G=
ENST00000053867.7:c.1179+12G= ENSP00000053867.2:n.1179+12G=
ENST00000586443.1:c.620+12G=
ENST00000589265.5:c.708+12G= ENSP00000467616.1:n.708+12G=
NM_002087.3:c.1179+12G= NP_002078.1:n.1179+12G=
XM_005257253.1:c.1179+12G= XP_005257310.1:n.1179+12G=
XM_024450730.1:c.1179+12G= XP_024306498.1:n.1179+12G=
NM_002087.4:c.1179+12G= MANE Select NP_002078.1:n.1179+12G=
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