Canonical Allele Identifier: CA1714174629
Gene: KCTD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66633624_66633628delinsAAGAC , CM000669.2:g.66633624_66633628delinsAAGAC GRCh38
NC_000007.13:g.66098611_66098615delinsAAGAC , CM000669.1:g.66098611_66098615delinsAAGAC GRCh37
NC_000007.12:g.65736046_65736050delinsAAGAC NCBI36
NG_028110.1:g.9744_9748delinsAAGAC
NG_028110.2:g.9744_9748delinsAAGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000275532.8:c.314+180_314+184delinsAAGAC ENSP00000275532.4:n.314+180_314+184delinsAAGAC
ENST00000449064.6:c.292+180_292+184delinsAAGAC
ENST00000503687.2:c.144+4416_144+4420delinsAAGAC ENSP00000421074.1:n.144+4416_144+4420delinsAAGAC
ENST00000638524.1:c.139+4416_139+4420delinsAAGAC
ENST00000638540.1:c.118+4416_118+4420delinsAAGAC
ENST00000639828.2:c.314+180_314+184delinsAAGAC MANE Select ENSP00000492240.1:n.314+180_314+184delinsAAGAC
ENST00000639879.1:c.314+180_314+184delinsAAGAC ENSP00000492161.1:n.314+180_314+184delinsAAGAC
ENST00000640234.1:c.184+180_184+184delinsAAGAC
ENST00000640385.1:c.314+180_314+184delinsAAGAC ENSP00000491193.1:n.314+180_314+184delinsAAGAC
ENST00000640851.1:c.314+180_314+184delinsAAGAC ENSP00000492577.1:n.314+180_314+184delinsAAGAC
ENST00000275532.7:c.314+180_314+184delinsAAGAC ENSP00000275532.3:n.314+180_314+184delinsAAGAC
ENST00000443322.1:c.314+180_314+184delinsAAGAC ENSP00000411624.1:n.314+180_314+184delinsAAGAC
ENST00000449064.5:c.144+4416_144+4420delinsAAGAC ENSP00000388463.1:n.144+4416_144+4420delinsAAGAC
ENST00000503687.1:c.144+4416_144+4420delinsAAGAC ENSP00000421074.1:n.144+4416_144+4420delinsAAGAC
NM_001167961.2:c.314+180_314+184delinsAAGAC NP_001161433.1:n.314+180_314+184delinsAAGAC
NM_153033.4:c.314+180_314+184delinsAAGAC NP_694578.1:n.314+180_314+184delinsAAGAC
NM_153033.5:c.314+180_314+184delinsAAGAC MANE Select NP_694578.1:n.314+180_314+184delinsAAGAC