Canonical Allele Identifier: CA1074912604
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

gnomAD v3: 5-34008137-A-AGCCG
gnomAD v4: 5-34008137-A-AGCCG
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008137_34008138insGCCG , CM000667.2:g.34008137_34008138insGCCG GRCh38
NC_000005.9:g.34008242_34008243insGCCG , CM000667.1:g.34008242_34008243insGCCG GRCh37
NC_000005.8:g.34043999_34044000insGCCG NCBI36
NG_016211.1:g.4978_4979insCGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2239_690-2238insCGGC ENSP00000371511.3:n.690-2239_690-2238insCGGC
NR_037951.1:n.765-2239_765-2238insCGGC
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