Canonical Allele Identifier: CA575145172

Gene: KCTD7

Linked Data

• gnomAD v2: 7-66098599-C-T
• gnomAD v3: 7-66633612-C-T
• gnomAD v4: 7-66633612-C-T
• MyVariant Identifiers: chr7:g.66098599C>T (hg19) ; chr7:g.66633612C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66633612C>T , CM000669.2:g.66633612C>T	GRCh38
NC_000007.13:g.66098599C>T , CM000669.1:g.66098599C>T	GRCh37
NC_000007.12:g.65736034C>T	NCBI36
NG_028110.1:g.9732C>T
NG_028110.2:g.9732C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275532.8:c.314+168C>T	ENSP00000275532.4:n.314+168C>T
ENST00000449064.6:c.292+168C>T
ENST00000503687.2:c.144+4404C>T	ENSP00000421074.1:n.144+4404C>T
ENST00000638524.1:c.139+4404C>T
ENST00000638540.1:c.118+4404C>T
ENST00000639828.2:c.314+168C>T MANE Select	ENSP00000492240.1:n.314+168C>T
ENST00000639879.1:c.314+168C>T	ENSP00000492161.1:n.314+168C>T
ENST00000640234.1:c.184+168C>T
ENST00000640385.1:c.314+168C>T	ENSP00000491193.1:n.314+168C>T
ENST00000640851.1:c.314+168C>T	ENSP00000492577.1:n.314+168C>T
ENST00000275532.7:c.314+168C>T	ENSP00000275532.3:n.314+168C>T
ENST00000443322.1:c.314+168C>T	ENSP00000411624.1:n.314+168C>T
ENST00000449064.5:c.144+4404C>T	ENSP00000388463.1:n.144+4404C>T
ENST00000503687.1:c.144+4404C>T	ENSP00000421074.1:n.144+4404C>T
NM_001167961.2:c.314+168C>T	NP_001161433.1:n.314+168C>T
NM_153033.4:c.314+168C>T	NP_694578.1:n.314+168C>T
NM_153033.5:c.314+168C>T MANE Select	NP_694578.1:n.314+168C>T