Canonical Allele Identifier: CA2673482032
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

gnomAD v4: 5-34008134-C-CCCAGCCGCGGCGCCGCGCCT
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008135_34008136insCAGCCGCGGCGCCGCGCCTC , CM000667.2:g.34008135_34008136insCAGCCGCGGCGCCGCGCCTC GRCh38
NC_000005.9:g.34008240_34008241insCAGCCGCGGCGCCGCGCCTC , CM000667.1:g.34008240_34008241insCAGCCGCGGCGCCGCGCCTC GRCh37
NC_000005.8:g.34043997_34043998insCAGCCGCGGCGCCGCGCCTC NCBI36
NG_016211.1:g.4981_4982insAGGCGCGGCGCCGCGGCTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2236_690-2235insAGGCGCGGCGCCGCGGCTGG ENSP00000371511.3:n.690-2236_690-2235insAGGCGCGGCGCCGCGGCTGG
NR_037951.1:n.765-2236_765-2235insAGGCGCGGCGCCGCGGCTGG
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