Canonical Allele Identifier: CA291853

Gene: KCTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66639241G>T , CM000669.2:g.66639241G>T	GRCh38
NC_000007.13:g.66104228G>T , CM000669.1:g.66104228G>T	GRCh37
NC_000007.12:g.65741663G>T	NCBI36
NG_028110.1:g.15361G>T
NG_028110.2:g.15361G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_153033.5:c.*9G>T MANE Select	NP_694578.1:n.*9G>T
ENST00000639828.2:c.*9G>T MANE Select	ENSP00000492240.1:n.*9G>T
NM_001167961.2:c.866+13G>T	NP_001161433.1:n.866+13G>T
NM_153033.4:c.*9G>T	NP_694578.1:n.*9G>T
ENST00000275532.7:c.*9G>T	ENSP00000275532.3:n.*9G>T
ENST00000275532.8:c.*62G>T	ENSP00000275532.4:n.*62G>T
ENST00000443322.1:c.866+13G>T	ENSP00000411624.1:n.866+13G>T
ENST00000449064.6:c.505+312G>T
ENST00000503687.1:c.397+312G>T	ENSP00000421074.1:n.397+312G>T
ENST00000503687.2:c.397+312G>T	ENSP00000421074.1:n.397+312G>T
ENST00000638524.1:c.691+13G>T
ENST00000638540.1:c.683G>T
ENST00000639879.1:c.*742G>T	ENSP00000492161.1:n.*742G>T
ENST00000640234.1:c.437+312G>T
ENST00000640385.1:c.866+13G>T	ENSP00000491193.1:n.866+13G>T
ENST00000640601.1:c.373+13G>T
ENST00000640851.1:c.668+13G>T	ENSP00000492577.1:n.668+13G>T