Canonical Allele Identifier: CA1714174613

Gene: KCTD7

Linked Data

• dbSNP Id: rs200176641
• gnomAD v4: 7-66633594-T-TATA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633594_66633595insATA , CM000669.2:g.66633594_66633595insATA	GRCh38
NC_000007.13:g.66098581_66098582insATA , CM000669.1:g.66098581_66098582insATA	GRCh37
NC_000007.12:g.65736016_65736017insATA	NCBI36
NG_028110.1:g.9714_9715insATA
NG_028110.2:g.9714_9715insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.314+150_314+151insATA	ENSP00000275532.4:n.314+150_314+151insATA
ENST00000449064.6:c.292+150_292+151insATA
ENST00000503687.2:c.144+4386_144+4387insATA	ENSP00000421074.1:n.144+4386_144+4387insATA
ENST00000638524.1:c.139+4386_139+4387insATA
ENST00000638540.1:c.118+4386_118+4387insATA
ENST00000639828.2:c.314+150_314+151insATA MANE Select	ENSP00000492240.1:n.314+150_314+151insATA
ENST00000639879.1:c.314+150_314+151insATA	ENSP00000492161.1:n.314+150_314+151insATA
ENST00000640234.1:c.184+150_184+151insATA
ENST00000640385.1:c.314+150_314+151insATA	ENSP00000491193.1:n.314+150_314+151insATA
ENST00000640851.1:c.314+150_314+151insATA	ENSP00000492577.1:n.314+150_314+151insATA
ENST00000275532.7:c.314+150_314+151insATA	ENSP00000275532.3:n.314+150_314+151insATA
ENST00000443322.1:c.314+150_314+151insATA	ENSP00000411624.1:n.314+150_314+151insATA
ENST00000449064.5:c.144+4386_144+4387insATA	ENSP00000388463.1:n.144+4386_144+4387insATA
ENST00000503687.1:c.144+4386_144+4387insATA	ENSP00000421074.1:n.144+4386_144+4387insATA
NM_001167961.2:c.314+150_314+151insATA	NP_001161433.1:n.314+150_314+151insATA
NM_153033.4:c.314+150_314+151insATA	NP_694578.1:n.314+150_314+151insATA
NM_153033.5:c.314+150_314+151insATA MANE Select	NP_694578.1:n.314+150_314+151insATA