Canonical Allele Identifier: CA160219758

Gene: KCTD7

Linked Data

• dbSNP Id: rs1491567562
• gnomAD v4: 7-66633592-AAT-A
• MyVariant Identifiers: chr7:g.66098580_66098581del (hg19) ; chr7:g.66633593_66633594del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633593_66633594del , CM000669.2:g.66633593_66633594del	GRCh38
NC_000007.13:g.66098580_66098581del , CM000669.1:g.66098580_66098581del	GRCh37
NC_000007.12:g.65736015_65736016del	NCBI36
NG_028110.1:g.9713_9714del
NG_028110.2:g.9713_9714del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.314+149_314+150del	ENSP00000275532.4:n.314+149_314+150del
ENST00000449064.6:c.292+149_292+150del
ENST00000503687.2:c.144+4385_144+4386del	ENSP00000421074.1:n.144+4385_144+4386del
ENST00000638524.1:c.139+4385_139+4386del
ENST00000638540.1:c.118+4385_118+4386del
ENST00000639828.2:c.314+149_314+150del MANE Select	ENSP00000492240.1:n.314+149_314+150del
ENST00000639879.1:c.314+149_314+150del	ENSP00000492161.1:n.314+149_314+150del
ENST00000640234.1:c.184+149_184+150del
ENST00000640385.1:c.314+149_314+150del	ENSP00000491193.1:n.314+149_314+150del
ENST00000640851.1:c.314+149_314+150del	ENSP00000492577.1:n.314+149_314+150del
ENST00000275532.7:c.314+149_314+150del	ENSP00000275532.3:n.314+149_314+150del
ENST00000443322.1:c.314+149_314+150del	ENSP00000411624.1:n.314+149_314+150del
ENST00000449064.5:c.144+4385_144+4386del	ENSP00000388463.1:n.144+4385_144+4386del
ENST00000503687.1:c.144+4385_144+4386del	ENSP00000421074.1:n.144+4385_144+4386del
NM_001167961.2:c.314+149_314+150del	NP_001161433.1:n.314+149_314+150del
NM_153033.4:c.314+149_314+150del	NP_694578.1:n.314+149_314+150del
NM_153033.5:c.314+149_314+150del MANE Select	NP_694578.1:n.314+149_314+150del