Canonical Allele Identifier: CA1102440420
Gene: KCTD7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66633611_66633615del , CM000669.2:g.66633611_66633615del GRCh38
NC_000007.13:g.66098598_66098602del , CM000669.1:g.66098598_66098602del GRCh37
NC_000007.12:g.65736033_65736037del NCBI36
NG_028110.1:g.9731_9735del
NG_028110.2:g.9731_9735del

Transcript Alleles

HGVS Amino-acid Change
ENST00000275532.8:c.314+167_314+171del ENSP00000275532.4:n.314+167_314+171del
ENST00000449064.6:c.292+167_292+171del
ENST00000503687.2:c.144+4403_144+4407del ENSP00000421074.1:n.144+4403_144+4407del
ENST00000638524.1:c.139+4403_139+4407del
ENST00000638540.1:c.118+4403_118+4407del
ENST00000639828.2:c.314+167_314+171del MANE Select ENSP00000492240.1:n.314+167_314+171del
ENST00000639879.1:c.314+167_314+171del ENSP00000492161.1:n.314+167_314+171del
ENST00000640234.1:c.184+167_184+171del
ENST00000640385.1:c.314+167_314+171del ENSP00000491193.1:n.314+167_314+171del
ENST00000640851.1:c.314+167_314+171del ENSP00000492577.1:n.314+167_314+171del
ENST00000275532.7:c.314+167_314+171del ENSP00000275532.3:n.314+167_314+171del
ENST00000443322.1:c.314+167_314+171del ENSP00000411624.1:n.314+167_314+171del
ENST00000449064.5:c.144+4403_144+4407del ENSP00000388463.1:n.144+4403_144+4407del
ENST00000503687.1:c.144+4403_144+4407del ENSP00000421074.1:n.144+4403_144+4407del
NM_001167961.2:c.314+167_314+171del NP_001161433.1:n.314+167_314+171del
NM_153033.4:c.314+167_314+171del NP_694578.1:n.314+167_314+171del
NM_153033.5:c.314+167_314+171del MANE Select NP_694578.1:n.314+167_314+171del