Canonical Allele Identifier: CA2683113835
Gene: KCTD7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66633594_66633595insATTTTTT , CM000669.2:g.66633594_66633595insATTTTTT GRCh38
NC_000007.13:g.66098581_66098582insATTTTTT , CM000669.1:g.66098581_66098582insATTTTTT GRCh37
NC_000007.12:g.65736016_65736017insATTTTTT NCBI36
NG_028110.1:g.9714_9715insATTTTTT
NG_028110.2:g.9714_9715insATTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000275532.8:c.314+150_314+151insATTTTTT ENSP00000275532.4:n.314+150_314+151insATTTTTT
ENST00000449064.6:c.292+150_292+151insATTTTTT
ENST00000503687.2:c.144+4386_144+4387insATTTTTT ENSP00000421074.1:n.144+4386_144+4387insATTTTTT
ENST00000638524.1:c.139+4386_139+4387insATTTTTT
ENST00000638540.1:c.118+4386_118+4387insATTTTTT
ENST00000639828.2:c.314+150_314+151insATTTTTT MANE Select ENSP00000492240.1:n.314+150_314+151insATTTTTT
ENST00000639879.1:c.314+150_314+151insATTTTTT ENSP00000492161.1:n.314+150_314+151insATTTTTT
ENST00000640234.1:c.184+150_184+151insATTTTTT
ENST00000640385.1:c.314+150_314+151insATTTTTT ENSP00000491193.1:n.314+150_314+151insATTTTTT
ENST00000640851.1:c.314+150_314+151insATTTTTT ENSP00000492577.1:n.314+150_314+151insATTTTTT
ENST00000275532.7:c.314+150_314+151insATTTTTT ENSP00000275532.3:n.314+150_314+151insATTTTTT
ENST00000443322.1:c.314+150_314+151insATTTTTT ENSP00000411624.1:n.314+150_314+151insATTTTTT
ENST00000449064.5:c.144+4386_144+4387insATTTTTT ENSP00000388463.1:n.144+4386_144+4387insATTTTTT
ENST00000503687.1:c.144+4386_144+4387insATTTTTT ENSP00000421074.1:n.144+4386_144+4387insATTTTTT
NM_001167961.2:c.314+150_314+151insATTTTTT NP_001161433.1:n.314+150_314+151insATTTTTT
NM_153033.4:c.314+150_314+151insATTTTTT NP_694578.1:n.314+150_314+151insATTTTTT
NM_153033.5:c.314+150_314+151insATTTTTT MANE Select NP_694578.1:n.314+150_314+151insATTTTTT