Canonical Allele Identifier: CA399769150
Gene: GRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42429554C>A (hg19) chr17:g.44352186C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44352186C>A , CM000679.2:g.44352186C>A GRCh38
NC_000017.10:g.42429554C>A , CM000679.1:g.42429554C>A GRCh37
NC_000017.9:g.39785080C>A NCBI36
NG_007886.1:g.12064C>A , LRG_661:g.12064C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1351C>A MANE Select ENSP00000053867.2:p.Pro451Thr
ENST00000639447.1:c.1137-343C>A ENSP00000492014.1:n.1137-343C>A
ENST00000053867.7:c.1351C>A ENSP00000053867.2:p.Pro451Thr
ENST00000586443.1:c.792C>A
ENST00000589265.5:c.880C>A ENSP00000467616.1:p.Pro294Thr
NM_002087.3:c.1351C>A NP_002078.1:p.Pro451Thr
XM_005257253.1:c.1351C>A XP_005257310.1:p.Pro451Thr
XM_024450730.1:c.1351C>A XP_024306498.1:p.Pro451Thr
NM_002087.4:c.1351C>A MANE Select NP_002078.1:p.Pro451Thr
Search 100 bp 5'
Search 100 bp 3'