Canonical Allele Identifier: CA1714178694

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66638857C= , CM000669.2:g.66638857C=	GRCh38
NC_000007.13:g.66103844C= , CM000669.1:g.66103844C=	GRCh37
NC_000007.12:g.65741279C=	NCBI36
NG_028110.1:g.14977C=
NG_028110.2:g.14977C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.455C=	ENSP00000275532.4:p.Thr152=
ENST00000449064.6:c.433C=
ENST00000503687.2:c.325C=	ENSP00000421074.1:p.Pro109=
ENST00000638524.1:c.320C=
ENST00000638540.1:c.299C=
ENST00000639828.2:c.495C= MANE Select	ENSP00000492240.1:p.Asp165=
ENST00000639879.1:c.*358C=	ENSP00000492161.1:n.*358C=
ENST00000640234.1:c.365C=
ENST00000640385.1:c.495C=	ENSP00000491193.1:p.Asp165=
ENST00000640601.1:c.2C=
ENST00000640851.1:c.495C=	ENSP00000492577.1:p.Asp165=
ENST00000275532.7:c.495C=	ENSP00000275532.3:p.Asp165=
ENST00000443322.1:c.495C=	ENSP00000411624.1:p.Asp165=
ENST00000449064.5:c.325C=	ENSP00000388463.1:p.Pro109=
ENST00000503687.1:c.325C=	ENSP00000421074.1:p.Pro109=
NM_001167961.2:c.495C=	NP_001161433.1:p.Asp165=
NM_153033.4:c.495C=	NP_694578.1:p.Asp165=
NM_153033.5:c.495C= MANE Select	NP_694578.1:p.Asp165=