Canonical Allele Identifier: CA1714178843

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66638962C= , CM000669.2:g.66638962C=	GRCh38
NC_000007.13:g.66103949C= , CM000669.1:g.66103949C=	GRCh37
NC_000007.12:g.65741384C=	NCBI36
NG_028110.1:g.15082C=
NG_028110.2:g.15082C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.560C=	ENSP00000275532.4:p.Pro187=
ENST00000449064.6:c.505+33C=
ENST00000503687.2:c.397+33C=	ENSP00000421074.1:n.397+33C=
ENST00000638524.1:c.425C=
ENST00000638540.1:c.404C=
ENST00000639828.2:c.600C= MANE Select	ENSP00000492240.1:p.Thr200=
ENST00000639879.1:c.*463C=	ENSP00000492161.1:n.*463C=
ENST00000640234.1:c.437+33C=
ENST00000640385.1:c.600C=	ENSP00000491193.1:p.Thr200=
ENST00000640601.1:c.107C=
ENST00000640851.1:c.567+33C=	ENSP00000492577.1:n.567+33C=
ENST00000275532.7:c.600C=	ENSP00000275532.3:p.Thr200=
ENST00000443322.1:c.600C=	ENSP00000411624.1:p.Thr200=
ENST00000503687.1:c.397+33C=	ENSP00000421074.1:n.397+33C=
NM_001167961.2:c.600C=	NP_001161433.1:p.Thr200=
NM_153033.4:c.600C=	NP_694578.1:p.Thr200=
NM_153033.5:c.600C= MANE Select	NP_694578.1:p.Thr200=