Canonical Allele Identifier: CA1102440536
Gene: KCTD7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66633621_66633622insTTTTTATTTTT , CM000669.2:g.66633621_66633622insTTTTTATTTTT GRCh38
NC_000007.13:g.66098608_66098609insTTTTTATTTTT , CM000669.1:g.66098608_66098609insTTTTTATTTTT GRCh37
NC_000007.12:g.65736043_65736044insTTTTTATTTTT NCBI36
NG_028110.1:g.9741_9742insTTTTTATTTTT
NG_028110.2:g.9741_9742insTTTTTATTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000275532.8:c.314+177_314+178insTTTTTATTTTT ENSP00000275532.4:n.314+177_314+178insTTTTTATTTTT
ENST00000449064.6:c.292+177_292+178insTTTTTATTTTT
ENST00000503687.2:c.144+4413_144+4414insTTTTTATTTTT ENSP00000421074.1:n.144+4413_144+4414insTTTTTATTTTT
ENST00000638524.1:c.139+4413_139+4414insTTTTTATTTTT
ENST00000638540.1:c.118+4413_118+4414insTTTTTATTTTT
ENST00000639828.2:c.314+177_314+178insTTTTTATTTTT MANE Select ENSP00000492240.1:n.314+177_314+178insTTTTTATTTTT
ENST00000639879.1:c.314+177_314+178insTTTTTATTTTT ENSP00000492161.1:n.314+177_314+178insTTTTTATTTTT
ENST00000640234.1:c.184+177_184+178insTTTTTATTTTT
ENST00000640385.1:c.314+177_314+178insTTTTTATTTTT ENSP00000491193.1:n.314+177_314+178insTTTTTATTTTT
ENST00000640851.1:c.314+177_314+178insTTTTTATTTTT ENSP00000492577.1:n.314+177_314+178insTTTTTATTTTT
ENST00000275532.7:c.314+177_314+178insTTTTTATTTTT ENSP00000275532.3:n.314+177_314+178insTTTTTATTTTT
ENST00000443322.1:c.314+177_314+178insTTTTTATTTTT ENSP00000411624.1:n.314+177_314+178insTTTTTATTTTT
ENST00000449064.5:c.144+4413_144+4414insTTTTTATTTTT ENSP00000388463.1:n.144+4413_144+4414insTTTTTATTTTT
ENST00000503687.1:c.144+4413_144+4414insTTTTTATTTTT ENSP00000421074.1:n.144+4413_144+4414insTTTTTATTTTT
NM_001167961.2:c.314+177_314+178insTTTTTATTTTT NP_001161433.1:n.314+177_314+178insTTTTTATTTTT
NM_153033.4:c.314+177_314+178insTTTTTATTTTT NP_694578.1:n.314+177_314+178insTTTTTATTTTT
NM_153033.5:c.314+177_314+178insTTTTTATTTTT MANE Select NP_694578.1:n.314+177_314+178insTTTTTATTTTT