Canonical Allele Identifier: CA2261354338
Gene: GRN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44351800A= , CM000679.2:g.44351800A= GRCh38
NC_000017.10:g.42429168A= , CM000679.1:g.42429168A= GRCh37
NC_000017.9:g.39784694A= NCBI36
NG_007886.1:g.11678A= , LRG_661:g.11678A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1179+5A= MANE Select ENSP00000053867.2:n.1179+5A=
ENST00000639447.1:c.1136+48A= ENSP00000492014.1:n.1136+48A=
ENST00000053867.7:c.1179+5A= ENSP00000053867.2:n.1179+5A=
ENST00000586443.1:c.620+5A=
ENST00000589265.5:c.708+5A= ENSP00000467616.1:n.708+5A=
NM_002087.3:c.1179+5A= NP_002078.1:n.1179+5A=
XM_005257253.1:c.1179+5A= XP_005257310.1:n.1179+5A=
XM_024450730.1:c.1179+5A= XP_024306498.1:n.1179+5A=
NM_002087.4:c.1179+5A= MANE Select NP_002078.1:n.1179+5A=
Search 100 bp 5'
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