Canonical Allele Identifier: CA841312644

Gene: KCTD7

Linked Data

• dbSNP Id: rs1241463748
• gnomAD v3: 7-66630986-TATCTG-T
• gnomAD v4: 7-66630986-TATCTG-T
• MyVariant Identifiers: chr7:g.66095974_66095978del (hg19) ; chr7:g.66630987_66630991del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66630988_66630992del , CM000669.2:g.66630988_66630992del	GRCh38
NC_000007.13:g.66095975_66095979del , CM000669.1:g.66095975_66095979del	GRCh37
NC_000007.12:g.65733410_65733414del	NCBI36
NG_028110.1:g.7108_7112del
NG_028110.2:g.7108_7112del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.144+1780_144+1784del	ENSP00000275532.4:n.144+1780_144+1784del
ENST00000449064.6:c.122+1780_122+1784del
ENST00000503687.2:c.144+1780_144+1784del	ENSP00000421074.1:n.144+1780_144+1784del
ENST00000638524.1:c.139+1780_139+1784del
ENST00000638540.1:c.118+1780_118+1784del
ENST00000639828.2:c.144+1780_144+1784del MANE Select	ENSP00000492240.1:n.144+1780_144+1784del
ENST00000639879.1:c.144+1780_144+1784del	ENSP00000492161.1:n.144+1780_144+1784del
ENST00000640234.1:c.14+1780_14+1784del
ENST00000640385.1:c.144+1780_144+1784del	ENSP00000491193.1:n.144+1780_144+1784del
ENST00000640851.1:c.144+1780_144+1784del	ENSP00000492577.1:n.144+1780_144+1784del
ENST00000275532.7:c.144+1780_144+1784del	ENSP00000275532.3:n.144+1780_144+1784del
ENST00000443322.1:c.144+1780_144+1784del	ENSP00000411624.1:n.144+1780_144+1784del
ENST00000449064.5:c.144+1780_144+1784del	ENSP00000388463.1:n.144+1780_144+1784del
ENST00000503687.1:c.144+1780_144+1784del	ENSP00000421074.1:n.144+1780_144+1784del
NM_001167961.2:c.144+1780_144+1784del	NP_001161433.1:n.144+1780_144+1784del
NM_153033.4:c.144+1780_144+1784del	NP_694578.1:n.144+1780_144+1784del
NM_153033.5:c.144+1780_144+1784del MANE Select	NP_694578.1:n.144+1780_144+1784del