Canonical Allele Identifier: CA1714173355
Gene: KCTD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.66630989C= , CM000669.2:g.66630989C= GRCh38
NC_000007.13:g.66095976C= , CM000669.1:g.66095976C= GRCh37
NC_000007.12:g.65733411C= NCBI36
NG_028110.1:g.7109C=
NG_028110.2:g.7109C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000275532.8:c.144+1781C= ENSP00000275532.4:n.144+1781C=
ENST00000449064.6:c.122+1781C=
ENST00000503687.2:c.144+1781C= ENSP00000421074.1:n.144+1781C=
ENST00000638524.1:c.139+1781C=
ENST00000638540.1:c.118+1781C=
ENST00000639828.2:c.144+1781C= MANE Select ENSP00000492240.1:n.144+1781C=
ENST00000639879.1:c.144+1781C= ENSP00000492161.1:n.144+1781C=
ENST00000640234.1:c.14+1781C=
ENST00000640385.1:c.144+1781C= ENSP00000491193.1:n.144+1781C=
ENST00000640851.1:c.144+1781C= ENSP00000492577.1:n.144+1781C=
ENST00000275532.7:c.144+1781C= ENSP00000275532.3:n.144+1781C=
ENST00000443322.1:c.144+1781C= ENSP00000411624.1:n.144+1781C=
ENST00000449064.5:c.144+1781C= ENSP00000388463.1:n.144+1781C=
ENST00000503687.1:c.144+1781C= ENSP00000421074.1:n.144+1781C=
NM_001167961.2:c.144+1781C= NP_001161433.1:n.144+1781C=
NM_153033.4:c.144+1781C= NP_694578.1:n.144+1781C=
NM_153033.5:c.144+1781C= MANE Select NP_694578.1:n.144+1781C=