Canonical Allele Identifier: CA841292966
Gene: KCTD7 HGNC NCBI

Linked Data

dbSNP Id: rs200130485

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66633609_66633610dup , CM000669.2:g.66633609_66633610dup GRCh38
NC_000007.13:g.66098596_66098597dup , CM000669.1:g.66098596_66098597dup GRCh37
NC_000007.12:g.65736031_65736032dup NCBI36
NG_028110.1:g.9729_9730dup
NG_028110.2:g.9729_9730dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000275532.8:c.314+165_314+166dup ENSP00000275532.4:n.314+165_314+166dup
ENST00000449064.6:c.292+165_292+166dup
ENST00000503687.2:c.144+4401_144+4402dup ENSP00000421074.1:n.144+4401_144+4402dup
ENST00000638524.1:c.139+4401_139+4402dup
ENST00000638540.1:c.118+4401_118+4402dup
ENST00000639828.2:c.314+165_314+166dup MANE Select ENSP00000492240.1:n.314+165_314+166dup
ENST00000639879.1:c.314+165_314+166dup ENSP00000492161.1:n.314+165_314+166dup
ENST00000640234.1:c.184+165_184+166dup
ENST00000640385.1:c.314+165_314+166dup ENSP00000491193.1:n.314+165_314+166dup
ENST00000640851.1:c.314+165_314+166dup ENSP00000492577.1:n.314+165_314+166dup
ENST00000275532.7:c.314+165_314+166dup ENSP00000275532.3:n.314+165_314+166dup
ENST00000443322.1:c.314+165_314+166dup ENSP00000411624.1:n.314+165_314+166dup
ENST00000449064.5:c.144+4401_144+4402dup ENSP00000388463.1:n.144+4401_144+4402dup
ENST00000503687.1:c.144+4401_144+4402dup ENSP00000421074.1:n.144+4401_144+4402dup
NM_001167961.2:c.314+165_314+166dup NP_001161433.1:n.314+165_314+166dup
NM_153033.4:c.314+165_314+166dup NP_694578.1:n.314+165_314+166dup
NM_153033.5:c.314+165_314+166dup MANE Select NP_694578.1:n.314+165_314+166dup