Canonical Allele Identifier: CA2776256313

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633581_66633582insA , CM000669.2:g.66633581_66633582insA	GRCh38
NC_000007.13:g.66098568_66098569insA , CM000669.1:g.66098568_66098569insA	GRCh37
NC_000007.12:g.65736003_65736004insA	NCBI36
NG_028110.1:g.9701_9702insA
NG_028110.2:g.9701_9702insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.314+137_314+138insA	ENSP00000275532.4:n.314+137_314+138insA
ENST00000449064.6:c.292+137_292+138insA
ENST00000503687.2:c.144+4373_144+4374insA	ENSP00000421074.1:n.144+4373_144+4374insA
ENST00000638524.1:c.139+4373_139+4374insA
ENST00000638540.1:c.118+4373_118+4374insA
ENST00000639828.2:c.314+137_314+138insA MANE Select	ENSP00000492240.1:n.314+137_314+138insA
ENST00000639879.1:c.314+137_314+138insA	ENSP00000492161.1:n.314+137_314+138insA
ENST00000640234.1:c.184+137_184+138insA
ENST00000640385.1:c.314+137_314+138insA	ENSP00000491193.1:n.314+137_314+138insA
ENST00000640851.1:c.314+137_314+138insA	ENSP00000492577.1:n.314+137_314+138insA
ENST00000275532.7:c.314+137_314+138insA	ENSP00000275532.3:n.314+137_314+138insA
ENST00000443322.1:c.314+137_314+138insA	ENSP00000411624.1:n.314+137_314+138insA
ENST00000449064.5:c.144+4373_144+4374insA	ENSP00000388463.1:n.144+4373_144+4374insA
ENST00000503687.1:c.144+4373_144+4374insA	ENSP00000421074.1:n.144+4373_144+4374insA
NM_001167961.2:c.314+137_314+138insA	NP_001161433.1:n.314+137_314+138insA
NM_153033.4:c.314+137_314+138insA	NP_694578.1:n.314+137_314+138insA
NM_153033.5:c.314+137_314+138insA MANE Select	NP_694578.1:n.314+137_314+138insA