Canonical Allele Identifier: CA1714174512

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633422G= , CM000669.2:g.66633422G=	GRCh38
NC_000007.13:g.66098409G= , CM000669.1:g.66098409G=	GRCh37
NC_000007.12:g.65735844G=	NCBI36
NG_028110.1:g.9542G=
NG_028110.2:g.9542G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000275532.8:c.292G=	ENSP00000275532.4:p.Asp98=
ENST00000449064.6:c.270G=
ENST00000503687.2:c.144+4214G=	ENSP00000421074.1:n.144+4214G=
ENST00000638524.1:c.139+4214G=
ENST00000638540.1:c.118+4214G=
ENST00000639828.2:c.292G= MANE Select	ENSP00000492240.1:p.Asp98=
ENST00000639879.1:c.292G=	ENSP00000492161.1:p.Asp98=
ENST00000640234.1:c.162G=
ENST00000640385.1:c.292G=	ENSP00000491193.1:p.Asp98=
ENST00000640851.1:c.292G=	ENSP00000492577.1:p.Asp98=
ENST00000275532.7:c.292G=	ENSP00000275532.3:p.Asp98=
ENST00000443322.1:c.292G=	ENSP00000411624.1:p.Asp98=
ENST00000449064.5:c.144+4214G=	ENSP00000388463.1:n.144+4214G=
ENST00000503687.1:c.144+4214G=	ENSP00000421074.1:n.144+4214G=
NM_001167961.2:c.292G=	NP_001161433.1:p.Asp98=
NM_153033.4:c.292G=	NP_694578.1:p.Asp98=
NM_153033.5:c.292G= MANE Select	NP_694578.1:p.Asp98=