Canonical Allele Identifier: CA1714173416

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66631108_66631112delinsCCTGT , CM000669.2:g.66631108_66631112delinsCCTGT	GRCh38
NC_000007.13:g.66096095_66096099delinsCCTGT , CM000669.1:g.66096095_66096099delinsCCTGT	GRCh37
NC_000007.12:g.65733530_65733534delinsCCTGT	NCBI36
NG_028110.1:g.7228_7232delinsCCTGT
NG_028110.2:g.7228_7232delinsCCTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000275532.8:c.144+1900_144+1904delinsCCTGT	ENSP00000275532.4:n.144+1900_144+1904delinsCCTGT
ENST00000449064.6:c.122+1900_122+1904delinsCCTGT
ENST00000503687.2:c.144+1900_144+1904delinsCCTGT	ENSP00000421074.1:n.144+1900_144+1904delinsCCTGT
ENST00000638524.1:c.139+1900_139+1904delinsCCTGT
ENST00000638540.1:c.118+1900_118+1904delinsCCTGT
ENST00000639828.2:c.144+1900_144+1904delinsCCTGT MANE Select	ENSP00000492240.1:n.144+1900_144+1904delinsCCTGT
ENST00000639879.1:c.144+1900_144+1904delinsCCTGT	ENSP00000492161.1:n.144+1900_144+1904delinsCCTGT
ENST00000640234.1:c.14+1900_14+1904delinsCCTGT
ENST00000640385.1:c.144+1900_144+1904delinsCCTGT	ENSP00000491193.1:n.144+1900_144+1904delinsCCTGT
ENST00000640851.1:c.144+1900_144+1904delinsCCTGT	ENSP00000492577.1:n.144+1900_144+1904delinsCCTGT
ENST00000275532.7:c.144+1900_144+1904delinsCCTGT	ENSP00000275532.3:n.144+1900_144+1904delinsCCTGT
ENST00000443322.1:c.144+1900_144+1904delinsCCTGT	ENSP00000411624.1:n.144+1900_144+1904delinsCCTGT
ENST00000449064.5:c.144+1900_144+1904delinsCCTGT	ENSP00000388463.1:n.144+1900_144+1904delinsCCTGT
ENST00000503687.1:c.144+1900_144+1904delinsCCTGT	ENSP00000421074.1:n.144+1900_144+1904delinsCCTGT
NM_001167961.2:c.144+1900_144+1904delinsCCTGT	NP_001161433.1:n.144+1900_144+1904delinsCCTGT
NM_153033.4:c.144+1900_144+1904delinsCCTGT	NP_694578.1:n.144+1900_144+1904delinsCCTGT
NM_153033.5:c.144+1900_144+1904delinsCCTGT MANE Select	NP_694578.1:n.144+1900_144+1904delinsCCTGT