Canonical Allele Identifier: CA1714174442

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633267_66633268delinsCT , CM000669.2:g.66633267_66633268delinsCT	GRCh38
NC_000007.13:g.66098254_66098255delinsCT , CM000669.1:g.66098254_66098255delinsCT	GRCh37
NC_000007.12:g.65735689_65735690delinsCT	NCBI36
NG_028110.1:g.9387_9388delinsCT
NG_028110.2:g.9387_9388delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.145-8_145-7delinsCT	ENSP00000275532.4:n.145-8_145-7delinsCT
ENST00000449064.6:c.123-8_123-7delinsCT
ENST00000503687.2:c.144+4059_144+4060delinsCT	ENSP00000421074.1:n.144+4059_144+4060delinsCT
ENST00000638524.1:c.139+4059_139+4060delinsCT
ENST00000638540.1:c.118+4059_118+4060delinsCT
ENST00000639828.2:c.145-8_145-7delinsCT MANE Select	ENSP00000492240.1:n.145-8_145-7delinsCT
ENST00000639879.1:c.145-8_145-7delinsCT	ENSP00000492161.1:n.145-8_145-7delinsCT
ENST00000640234.1:c.15-8_15-7delinsCT
ENST00000640385.1:c.145-8_145-7delinsCT	ENSP00000491193.1:n.145-8_145-7delinsCT
ENST00000640851.1:c.145-8_145-7delinsCT	ENSP00000492577.1:n.145-8_145-7delinsCT
ENST00000275532.7:c.145-8_145-7delinsCT	ENSP00000275532.3:n.145-8_145-7delinsCT
ENST00000443322.1:c.145-8_145-7delinsCT	ENSP00000411624.1:n.145-8_145-7delinsCT
ENST00000449064.5:c.144+4059_144+4060delinsCT	ENSP00000388463.1:n.144+4059_144+4060delinsCT
ENST00000503687.1:c.144+4059_144+4060delinsCT	ENSP00000421074.1:n.144+4059_144+4060delinsCT
NM_001167961.2:c.145-8_145-7delinsCT	NP_001161433.1:n.145-8_145-7delinsCT
NM_153033.4:c.145-8_145-7delinsCT	NP_694578.1:n.145-8_145-7delinsCT
NM_153033.5:c.145-8_145-7delinsCT MANE Select	NP_694578.1:n.145-8_145-7delinsCT