Canonical Allele Identifier: CA1102440491
Gene: KCTD7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66633615_66633616insTTTTT , CM000669.2:g.66633615_66633616insTTTTT GRCh38
NC_000007.13:g.66098602_66098603insTTTTT , CM000669.1:g.66098602_66098603insTTTTT GRCh37
NC_000007.12:g.65736037_65736038insTTTTT NCBI36
NG_028110.1:g.9735_9736insTTTTT
NG_028110.2:g.9735_9736insTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000275532.8:c.314+171_314+172insTTTTT ENSP00000275532.4:n.314+171_314+172insTTTTT
ENST00000449064.6:c.292+171_292+172insTTTTT
ENST00000503687.2:c.144+4407_144+4408insTTTTT ENSP00000421074.1:n.144+4407_144+4408insTTTTT
ENST00000638524.1:c.139+4407_139+4408insTTTTT
ENST00000638540.1:c.118+4407_118+4408insTTTTT
ENST00000639828.2:c.314+171_314+172insTTTTT MANE Select ENSP00000492240.1:n.314+171_314+172insTTTTT
ENST00000639879.1:c.314+171_314+172insTTTTT ENSP00000492161.1:n.314+171_314+172insTTTTT
ENST00000640234.1:c.184+171_184+172insTTTTT
ENST00000640385.1:c.314+171_314+172insTTTTT ENSP00000491193.1:n.314+171_314+172insTTTTT
ENST00000640851.1:c.314+171_314+172insTTTTT ENSP00000492577.1:n.314+171_314+172insTTTTT
ENST00000275532.7:c.314+171_314+172insTTTTT ENSP00000275532.3:n.314+171_314+172insTTTTT
ENST00000443322.1:c.314+171_314+172insTTTTT ENSP00000411624.1:n.314+171_314+172insTTTTT
ENST00000449064.5:c.144+4407_144+4408insTTTTT ENSP00000388463.1:n.144+4407_144+4408insTTTTT
ENST00000503687.1:c.144+4407_144+4408insTTTTT ENSP00000421074.1:n.144+4407_144+4408insTTTTT
NM_001167961.2:c.314+171_314+172insTTTTT NP_001161433.1:n.314+171_314+172insTTTTT
NM_153033.4:c.314+171_314+172insTTTTT NP_694578.1:n.314+171_314+172insTTTTT
NM_153033.5:c.314+171_314+172insTTTTT MANE Select NP_694578.1:n.314+171_314+172insTTTTT