Canonical Allele Identifier: CA160219769

Gene: KCTD7

Linked Data

• dbSNP Id: rs903362733
• gnomAD v2: 7-66098609-CAAAG-C
• gnomAD v3: 7-66633622-CAAAG-C
• gnomAD v4: 7-66633622-CAAAG-C
• MyVariant Identifiers: chr7:g.66098610_66098613del (hg19) ; chr7:g.66633623_66633626del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633624_66633627del , CM000669.2:g.66633624_66633627del	GRCh38
NC_000007.13:g.66098611_66098614del , CM000669.1:g.66098611_66098614del	GRCh37
NC_000007.12:g.65736046_65736049del	NCBI36
NG_028110.1:g.9744_9747del
NG_028110.2:g.9744_9747del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.314+180_314+183del	ENSP00000275532.4:n.314+180_314+183del
ENST00000449064.6:c.292+180_292+183del
ENST00000503687.2:c.144+4416_144+4419del	ENSP00000421074.1:n.144+4416_144+4419del
ENST00000638524.1:c.139+4416_139+4419del
ENST00000638540.1:c.118+4416_118+4419del
ENST00000639828.2:c.314+180_314+183del MANE Select	ENSP00000492240.1:n.314+180_314+183del
ENST00000639879.1:c.314+180_314+183del	ENSP00000492161.1:n.314+180_314+183del
ENST00000640234.1:c.184+180_184+183del
ENST00000640385.1:c.314+180_314+183del	ENSP00000491193.1:n.314+180_314+183del
ENST00000640851.1:c.314+180_314+183del	ENSP00000492577.1:n.314+180_314+183del
ENST00000275532.7:c.314+180_314+183del	ENSP00000275532.3:n.314+180_314+183del
ENST00000443322.1:c.314+180_314+183del	ENSP00000411624.1:n.314+180_314+183del
ENST00000449064.5:c.144+4416_144+4419del	ENSP00000388463.1:n.144+4416_144+4419del
ENST00000503687.1:c.144+4416_144+4419del	ENSP00000421074.1:n.144+4416_144+4419del
NM_001167961.2:c.314+180_314+183del	NP_001161433.1:n.314+180_314+183del
NM_153033.4:c.314+180_314+183del	NP_694578.1:n.314+180_314+183del
NM_153033.5:c.314+180_314+183del MANE Select	NP_694578.1:n.314+180_314+183del