Canonical Allele Identifier: CA1074912557
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

dbSNP Id: rs937490547

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008135_34008136insCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCC , CM000667.2:g.34008135_34008136insCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCC GRCh38
NC_000005.9:g.34008240_34008241insCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCC , CM000667.1:g.34008240_34008241insCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCC GRCh37
NC_000005.8:g.34043997_34043998insCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCCCAGCCGCGGCGCCGCGCCCC NCBI36
NG_016211.1:g.5006_5007insCGGCGCCGCGGCTGGGGGCGCGGCGCCGCGGCTGGGGGCGCGGCGCCGCGGCTGGGGGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2211_690-2210insCGGCGCCGCGGCTGGGGGCGCGGCGCCGCGGCTGGGGGCGCGGCGCCGCGGCTGGGGGCG ENSP00000371511.3:n.690-2211_690-2210insCGGCGCCGCGGCTGGGGGCGC...
NR_037951.1:n.765-2211_765-2210insCGGCGCCGCGGCTGGGGGCGCGGCGCCGCGGCTGGGGGCGCGGCGCCGCGGCTGGGGGCG