Canonical Allele Identifier: CA1714178699

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66638861T= , CM000669.2:g.66638861T=	GRCh38
NC_000007.13:g.66103848T= , CM000669.1:g.66103848T=	GRCh37
NC_000007.12:g.65741283T=	NCBI36
NG_028110.1:g.14981T=
NG_028110.2:g.14981T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000275532.8:c.459T=	ENSP00000275532.4:p.Thr153=
ENST00000449064.6:c.437T=
ENST00000503687.2:c.329T=	ENSP00000421074.1:p.Leu110=
ENST00000638524.1:c.324T=
ENST00000638540.1:c.303T=
ENST00000639828.2:c.499T= MANE Select	ENSP00000492240.1:p.Leu167=
ENST00000639879.1:c.*362T=	ENSP00000492161.1:n.*362T=
ENST00000640234.1:c.369T=
ENST00000640385.1:c.499T=	ENSP00000491193.1:p.Leu167=
ENST00000640601.1:c.6T=
ENST00000640851.1:c.499T=	ENSP00000492577.1:p.Leu167=
ENST00000275532.7:c.499T=	ENSP00000275532.3:p.Leu167=
ENST00000443322.1:c.499T=	ENSP00000411624.1:p.Leu167=
ENST00000449064.5:c.329T=	ENSP00000388463.1:p.Leu110=
ENST00000503687.1:c.329T=	ENSP00000421074.1:p.Leu110=
NM_001167961.2:c.499T=	NP_001161433.1:p.Leu167=
NM_153033.4:c.499T=	NP_694578.1:p.Leu167=
NM_153033.5:c.499T= MANE Select	NP_694578.1:p.Leu167=