Canonical Allele Identifier: CA1714178712

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66638868G= , CM000669.2:g.66638868G=	GRCh38
NC_000007.13:g.66103855G= , CM000669.1:g.66103855G=	GRCh37
NC_000007.12:g.65741290G=	NCBI36
NG_028110.1:g.14988G=
NG_028110.2:g.14988G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.466G=	ENSP00000275532.4:p.Gly156=
ENST00000449064.6:c.444G=
ENST00000503687.2:c.336G=	ENSP00000421074.1:p.Ala112=
ENST00000638524.1:c.331G=
ENST00000638540.1:c.310G=
ENST00000639828.2:c.506G= MANE Select	ENSP00000492240.1:p.Arg169=
ENST00000639879.1:c.*369G=	ENSP00000492161.1:n.*369G=
ENST00000640234.1:c.376G=
ENST00000640385.1:c.506G=	ENSP00000491193.1:p.Arg169=
ENST00000640601.1:c.13G=
ENST00000640851.1:c.506G=	ENSP00000492577.1:p.Arg169=
ENST00000275532.7:c.506G=	ENSP00000275532.3:p.Arg169=
ENST00000443322.1:c.506G=	ENSP00000411624.1:p.Arg169=
ENST00000449064.5:c.336G=	ENSP00000388463.1:p.Ala112=
ENST00000503687.1:c.336G=	ENSP00000421074.1:p.Ala112=
NM_001167961.2:c.506G=	NP_001161433.1:p.Arg169=
NM_153033.4:c.506G=	NP_694578.1:p.Arg169=
NM_153033.5:c.506G= MANE Select	NP_694578.1:p.Arg169=