Canonical Allele Identifier: CA2776256280

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633566_66633567insC , CM000669.2:g.66633566_66633567insC	GRCh38
NC_000007.13:g.66098553_66098554insC , CM000669.1:g.66098553_66098554insC	GRCh37
NC_000007.12:g.65735988_65735989insC	NCBI36
NG_028110.1:g.9686_9687insC
NG_028110.2:g.9686_9687insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.314+122_314+123insC	ENSP00000275532.4:n.314+122_314+123insC
ENST00000449064.6:c.292+122_292+123insC
ENST00000503687.2:c.144+4358_144+4359insC	ENSP00000421074.1:n.144+4358_144+4359insC
ENST00000638524.1:c.139+4358_139+4359insC
ENST00000638540.1:c.118+4358_118+4359insC
ENST00000639828.2:c.314+122_314+123insC MANE Select	ENSP00000492240.1:n.314+122_314+123insC
ENST00000639879.1:c.314+122_314+123insC	ENSP00000492161.1:n.314+122_314+123insC
ENST00000640234.1:c.184+122_184+123insC
ENST00000640385.1:c.314+122_314+123insC	ENSP00000491193.1:n.314+122_314+123insC
ENST00000640851.1:c.314+122_314+123insC	ENSP00000492577.1:n.314+122_314+123insC
ENST00000275532.7:c.314+122_314+123insC	ENSP00000275532.3:n.314+122_314+123insC
ENST00000443322.1:c.314+122_314+123insC	ENSP00000411624.1:n.314+122_314+123insC
ENST00000449064.5:c.144+4358_144+4359insC	ENSP00000388463.1:n.144+4358_144+4359insC
ENST00000503687.1:c.144+4358_144+4359insC	ENSP00000421074.1:n.144+4358_144+4359insC
NM_001167961.2:c.314+122_314+123insC	NP_001161433.1:n.314+122_314+123insC
NM_153033.4:c.314+122_314+123insC	NP_694578.1:n.314+122_314+123insC
NM_153033.5:c.314+122_314+123insC MANE Select	NP_694578.1:n.314+122_314+123insC