Canonical Allele Identifier: CA1714178708

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66638867C= , CM000669.2:g.66638867C=	GRCh38
NC_000007.13:g.66103854C= , CM000669.1:g.66103854C=	GRCh37
NC_000007.12:g.65741289C=	NCBI36
NG_028110.1:g.14987C=
NG_028110.2:g.14987C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000275532.8:c.465C=	ENSP00000275532.4:p.Ser155=
ENST00000449064.6:c.443C=
ENST00000503687.2:c.335C=	ENSP00000421074.1:p.Ala112=
ENST00000638524.1:c.330C=
ENST00000638540.1:c.309C=
ENST00000639828.2:c.505C= MANE Select	ENSP00000492240.1:p.Arg169=
ENST00000639879.1:c.*368C=	ENSP00000492161.1:n.*368C=
ENST00000640234.1:c.375C=
ENST00000640385.1:c.505C=	ENSP00000491193.1:p.Arg169=
ENST00000640601.1:c.12C=
ENST00000640851.1:c.505C=	ENSP00000492577.1:p.Arg169=
ENST00000275532.7:c.505C=	ENSP00000275532.3:p.Arg169=
ENST00000443322.1:c.505C=	ENSP00000411624.1:p.Arg169=
ENST00000449064.5:c.335C=	ENSP00000388463.1:p.Ala112=
ENST00000503687.1:c.335C=	ENSP00000421074.1:p.Ala112=
NM_001167961.2:c.505C=	NP_001161433.1:p.Arg169=
NM_153033.4:c.505C=	NP_694578.1:p.Arg169=
NM_153033.5:c.505C= MANE Select	NP_694578.1:p.Arg169=