Canonical Allele Identifier: CA2261354448
Gene: GRN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44351991_44351992delinsCG , CM000679.2:g.44351991_44351992delinsCG GRCh38
NC_000017.10:g.42429359_42429360delinsCG , CM000679.1:g.42429359_42429360delinsCG GRCh37
NC_000017.9:g.39784885_39784886delinsCG NCBI36
NG_007886.1:g.11869_11870delinsCG , LRG_661:g.11869_11870delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000053867.8:c.1180-24_1180-23delinsCG MANE Select ENSP00000053867.2:n.1180-24_1180-23delins...
ENST00000639447.1:c.1136+239_1136+240delinsCG ENSP00000492014.1:n.1136+239_1136+240deli...
ENST00000053867.7:c.1180-24_1180-23delinsCG ENSP00000053867.2:n.1180-24_1180-23delins...
ENST00000586443.1:c.621-24_621-23delinsCG
ENST00000589265.5:c.709-24_709-23delinsCG ENSP00000467616.1:n.709-24_709-23delinsCG...
NM_002087.3:c.1180-24_1180-23delinsCG NP_002078.1:n.1180-24_1180-23delinsCG
XM_005257253.1:c.1180-24_1180-23delinsCG XP_005257310.1:n.1180-24_1180-23delinsCG
XM_024450730.1:c.1180-24_1180-23delinsCG XP_024306498.1:n.1180-24_1180-23delinsCG
NM_002087.4:c.1180-24_1180-23delinsCG MANE Select NP_002078.1:n.1180-24_1180-23delinsCG
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