Canonical Allele Identifier: CA2638210865
Gene: GRN HGNC NCBI

Linked Data

gnomAD v4: 17-44352314-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44352314G>A , CM000679.2:g.44352314G>A GRCh38
NC_000017.10:g.42429682G>A , CM000679.1:g.42429682G>A GRCh37
NC_000017.9:g.39785208G>A NCBI36
NG_007886.1:g.12192G>A , LRG_661:g.12192G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1414-27G>A MANE Select ENSP00000053867.2:n.1414-27G>A
ENST00000639447.1:c.1137-215G>A ENSP00000492014.1:n.1137-215G>A
ENST00000053867.7:c.1414-27G>A ENSP00000053867.2:n.1414-27G>A
ENST00000586242.1:c.48-27G>A
ENST00000586443.1:c.855-27G>A
ENST00000589265.5:c.943-27G>A ENSP00000467616.1:n.943-27G>A
NM_002087.3:c.1414-27G>A NP_002078.1:n.1414-27G>A
XM_005257253.1:c.1414-27G>A XP_005257310.1:n.1414-27G>A
XM_024450730.1:c.1414-27G>A XP_024306498.1:n.1414-27G>A
NM_002087.4:c.1414-27G>A MANE Select NP_002078.1:n.1414-27G>A
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