Canonical Allele Identifier: CA2776256329

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633590_66633591insAC , CM000669.2:g.66633590_66633591insAC	GRCh38
NC_000007.13:g.66098577_66098578insAC , CM000669.1:g.66098577_66098578insAC	GRCh37
NC_000007.12:g.65736012_65736013insAC	NCBI36
NG_028110.1:g.9710_9711insAC
NG_028110.2:g.9710_9711insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.314+146_314+147insAC	ENSP00000275532.4:n.314+146_314+147insAC
ENST00000449064.6:c.292+146_292+147insAC
ENST00000503687.2:c.144+4382_144+4383insAC	ENSP00000421074.1:n.144+4382_144+4383insAC
ENST00000638524.1:c.139+4382_139+4383insAC
ENST00000638540.1:c.118+4382_118+4383insAC
ENST00000639828.2:c.314+146_314+147insAC MANE Select	ENSP00000492240.1:n.314+146_314+147insAC
ENST00000639879.1:c.314+146_314+147insAC	ENSP00000492161.1:n.314+146_314+147insAC
ENST00000640234.1:c.184+146_184+147insAC
ENST00000640385.1:c.314+146_314+147insAC	ENSP00000491193.1:n.314+146_314+147insAC
ENST00000640851.1:c.314+146_314+147insAC	ENSP00000492577.1:n.314+146_314+147insAC
ENST00000275532.7:c.314+146_314+147insAC	ENSP00000275532.3:n.314+146_314+147insAC
ENST00000443322.1:c.314+146_314+147insAC	ENSP00000411624.1:n.314+146_314+147insAC
ENST00000449064.5:c.144+4382_144+4383insAC	ENSP00000388463.1:n.144+4382_144+4383insAC
ENST00000503687.1:c.144+4382_144+4383insAC	ENSP00000421074.1:n.144+4382_144+4383insAC
NM_001167961.2:c.314+146_314+147insAC	NP_001161433.1:n.314+146_314+147insAC
NM_153033.4:c.314+146_314+147insAC	NP_694578.1:n.314+146_314+147insAC
NM_153033.5:c.314+146_314+147insAC MANE Select	NP_694578.1:n.314+146_314+147insAC