Canonical Allele Identifier: CA1714178846

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66638965C= , CM000669.2:g.66638965C=	GRCh38
NC_000007.13:g.66103952C= , CM000669.1:g.66103952C=	GRCh37
NC_000007.12:g.65741387C=	NCBI36
NG_028110.1:g.15085C=
NG_028110.2:g.15085C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000275532.8:c.563C=	ENSP00000275532.4:p.Pro188=
ENST00000449064.6:c.505+36C=
ENST00000503687.2:c.397+36C=	ENSP00000421074.1:n.397+36C=
ENST00000638524.1:c.428C=
ENST00000638540.1:c.407C=
ENST00000639828.2:c.603C= MANE Select	ENSP00000492240.1:p.Pro201=
ENST00000639879.1:c.*466C=	ENSP00000492161.1:n.*466C=
ENST00000640234.1:c.437+36C=
ENST00000640385.1:c.603C=	ENSP00000491193.1:p.Pro201=
ENST00000640601.1:c.110C=
ENST00000640851.1:c.567+36C=	ENSP00000492577.1:n.567+36C=
ENST00000275532.7:c.603C=	ENSP00000275532.3:p.Pro201=
ENST00000443322.1:c.603C=	ENSP00000411624.1:p.Pro201=
ENST00000503687.1:c.397+36C=	ENSP00000421074.1:n.397+36C=
NM_001167961.2:c.603C=	NP_001161433.1:p.Pro201=
NM_153033.4:c.603C=	NP_694578.1:p.Pro201=
NM_153033.5:c.603C= MANE Select	NP_694578.1:p.Pro201=