Canonical Allele Identifier: CA1714174646

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633673_66633674delinsTC , CM000669.2:g.66633673_66633674delinsTC	GRCh38
NC_000007.13:g.66098660_66098661delinsTC , CM000669.1:g.66098660_66098661delinsTC	GRCh37
NC_000007.12:g.65736095_65736096delinsTC	NCBI36
NG_028110.1:g.9793_9794delinsTC
NG_028110.2:g.9793_9794delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.314+229_314+230delinsTC	ENSP00000275532.4:n.314+229_314+230delinsTC
ENST00000449064.6:c.292+229_292+230delinsTC
ENST00000503687.2:c.144+4465_144+4466delinsTC	ENSP00000421074.1:n.144+4465_144+4466delinsTC
ENST00000638524.1:c.139+4465_139+4466delinsTC
ENST00000638540.1:c.118+4465_118+4466delinsTC
ENST00000639828.2:c.314+229_314+230delinsTC MANE Select	ENSP00000492240.1:n.314+229_314+230delinsTC
ENST00000639879.1:c.314+229_314+230delinsTC	ENSP00000492161.1:n.314+229_314+230delinsTC
ENST00000640234.1:c.184+229_184+230delinsTC
ENST00000640385.1:c.314+229_314+230delinsTC	ENSP00000491193.1:n.314+229_314+230delinsTC
ENST00000640851.1:c.314+229_314+230delinsTC	ENSP00000492577.1:n.314+229_314+230delinsTC
ENST00000275532.7:c.314+229_314+230delinsTC	ENSP00000275532.3:n.314+229_314+230delinsTC
ENST00000443322.1:c.314+229_314+230delinsTC	ENSP00000411624.1:n.314+229_314+230delinsTC
ENST00000449064.5:c.144+4465_144+4466delinsTC	ENSP00000388463.1:n.144+4465_144+4466delinsTC
ENST00000503687.1:c.144+4465_144+4466delinsTC	ENSP00000421074.1:n.144+4465_144+4466delinsTC
NM_001167961.2:c.314+229_314+230delinsTC	NP_001161433.1:n.314+229_314+230delinsTC
NM_153033.4:c.314+229_314+230delinsTC	NP_694578.1:n.314+229_314+230delinsTC
NM_153033.5:c.314+229_314+230delinsTC MANE Select	NP_694578.1:n.314+229_314+230delinsTC