Canonical Allele Identifier: CA2776256228

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633542_66633543insA , CM000669.2:g.66633542_66633543insA	GRCh38
NC_000007.13:g.66098529_66098530insA , CM000669.1:g.66098529_66098530insA	GRCh37
NC_000007.12:g.65735964_65735965insA	NCBI36
NG_028110.1:g.9662_9663insA
NG_028110.2:g.9662_9663insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.314+98_314+99insA	ENSP00000275532.4:n.314+98_314+99insA
ENST00000449064.6:c.292+98_292+99insA
ENST00000503687.2:c.144+4334_144+4335insA	ENSP00000421074.1:n.144+4334_144+4335insA
ENST00000638524.1:c.139+4334_139+4335insA
ENST00000638540.1:c.118+4334_118+4335insA
ENST00000639828.2:c.314+98_314+99insA MANE Select	ENSP00000492240.1:n.314+98_314+99insA
ENST00000639879.1:c.314+98_314+99insA	ENSP00000492161.1:n.314+98_314+99insA
ENST00000640234.1:c.184+98_184+99insA
ENST00000640385.1:c.314+98_314+99insA	ENSP00000491193.1:n.314+98_314+99insA
ENST00000640851.1:c.314+98_314+99insA	ENSP00000492577.1:n.314+98_314+99insA
ENST00000275532.7:c.314+98_314+99insA	ENSP00000275532.3:n.314+98_314+99insA
ENST00000443322.1:c.314+98_314+99insA	ENSP00000411624.1:n.314+98_314+99insA
ENST00000449064.5:c.144+4334_144+4335insA	ENSP00000388463.1:n.144+4334_144+4335insA
ENST00000503687.1:c.144+4334_144+4335insA	ENSP00000421074.1:n.144+4334_144+4335insA
NM_001167961.2:c.314+98_314+99insA	NP_001161433.1:n.314+98_314+99insA
NM_153033.4:c.314+98_314+99insA	NP_694578.1:n.314+98_314+99insA
NM_153033.5:c.314+98_314+99insA MANE Select	NP_694578.1:n.314+98_314+99insA