Canonical Allele Identifier: CA2261354414
Gene: GRN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44351948G= , CM000679.2:g.44351948G= GRCh38
NC_000017.10:g.42429316G= , CM000679.1:g.42429316G= GRCh37
NC_000017.9:g.39784842G= NCBI36
NG_007886.1:g.11826G= , LRG_661:g.11826G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1180-67G= MANE Select ENSP00000053867.2:n.1180-67G=
ENST00000639447.1:c.1136+196G= ENSP00000492014.1:n.1136+196G=
ENST00000053867.7:c.1180-67G= ENSP00000053867.2:n.1180-67G=
ENST00000586443.1:c.621-67G=
ENST00000589265.5:c.709-67G= ENSP00000467616.1:n.709-67G=
NM_002087.3:c.1180-67G= NP_002078.1:n.1180-67G=
XM_005257253.1:c.1180-67G= XP_005257310.1:n.1180-67G=
XM_024450730.1:c.1180-67G= XP_024306498.1:n.1180-67G=
NM_002087.4:c.1180-67G= MANE Select NP_002078.1:n.1180-67G=
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