Canonical Allele Identifier: CA2776256190

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633527_66633528insG , CM000669.2:g.66633527_66633528insG	GRCh38
NC_000007.13:g.66098514_66098515insG , CM000669.1:g.66098514_66098515insG	GRCh37
NC_000007.12:g.65735949_65735950insG	NCBI36
NG_028110.1:g.9647_9648insG
NG_028110.2:g.9647_9648insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.314+83_314+84insG	ENSP00000275532.4:n.314+83_314+84insG
ENST00000449064.6:c.292+83_292+84insG
ENST00000503687.2:c.144+4319_144+4320insG	ENSP00000421074.1:n.144+4319_144+4320insG
ENST00000638524.1:c.139+4319_139+4320insG
ENST00000638540.1:c.118+4319_118+4320insG
ENST00000639828.2:c.314+83_314+84insG MANE Select	ENSP00000492240.1:n.314+83_314+84insG
ENST00000639879.1:c.314+83_314+84insG	ENSP00000492161.1:n.314+83_314+84insG
ENST00000640234.1:c.184+83_184+84insG
ENST00000640385.1:c.314+83_314+84insG	ENSP00000491193.1:n.314+83_314+84insG
ENST00000640851.1:c.314+83_314+84insG	ENSP00000492577.1:n.314+83_314+84insG
ENST00000275532.7:c.314+83_314+84insG	ENSP00000275532.3:n.314+83_314+84insG
ENST00000443322.1:c.314+83_314+84insG	ENSP00000411624.1:n.314+83_314+84insG
ENST00000449064.5:c.144+4319_144+4320insG	ENSP00000388463.1:n.144+4319_144+4320insG
ENST00000503687.1:c.144+4319_144+4320insG	ENSP00000421074.1:n.144+4319_144+4320insG
NM_001167961.2:c.314+83_314+84insG	NP_001161433.1:n.314+83_314+84insG
NM_153033.4:c.314+83_314+84insG	NP_694578.1:n.314+83_314+84insG
NM_153033.5:c.314+83_314+84insG MANE Select	NP_694578.1:n.314+83_314+84insG