Canonical Allele Identifier: CA2638209979
Gene: GRN HGNC NCBI

Linked Data

gnomAD v4: 17-44351869-T-TA
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44351870dup , CM000679.2:g.44351870dup GRCh38
NC_000017.10:g.42429238dup , CM000679.1:g.42429238dup GRCh37
NC_000017.9:g.39784764dup NCBI36
NG_007886.1:g.11748dup , LRG_661:g.11748dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1179+75dup MANE Select ENSP00000053867.2:n.1179+75dup
ENST00000639447.1:c.1136+118dup ENSP00000492014.1:n.1136+118dup
ENST00000053867.7:c.1179+75dup ENSP00000053867.2:n.1179+75dup
ENST00000586443.1:c.620+75dup
ENST00000589265.5:c.708+75dup ENSP00000467616.1:n.708+75dup
NM_002087.3:c.1179+75dup NP_002078.1:n.1179+75dup
XM_005257253.1:c.1179+75dup XP_005257310.1:n.1179+75dup
XM_024450730.1:c.1179+75dup XP_024306498.1:n.1179+75dup
NM_002087.4:c.1179+75dup MANE Select NP_002078.1:n.1179+75dup
Search 100 bp 5'
Search 100 bp 3'