Canonical Allele Identifier: CA2601266799
Gene: C11orf97 HGNC NCBI

Linked Data

gnomAD v3: 11-94522027-CT-C
gnomAD v4: 11-94522027-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94522032del , CM000673.2:g.94522032del GRCh38
NC_000011.9:g.94255198del , CM000673.1:g.94255198del GRCh37
NC_000011.8:g.93894846del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000542198.3:c.250+4345del MANE Select ENSP00000490577.1:n.250+4345del
NM_001190462.1:c.250+4345del NP_001177391.1:n.250+4345del
NM_001190462.2:c.250+4345del MANE Select NP_001177391.1:n.250+4345del
Search 100 bp 5'
Search 100 bp 3'