Canonical Allele Identifier: CA1714173355

Gene: KCTD7

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=