Canonical Allele Identifier: CA1637932974

Gene: KCNQ5

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.72933566C>G , CM000668.2:g.72933566C>G	GRCh38
NC_000006.11:g.73643289C>G , CM000668.1:g.73643289C>G	GRCh37
NC_000006.10:g.73700010C>G	NCBI36
NG_047170.1:g.317287C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355194.9:c.399-70342C>G	ENSP00000347326.5:n.399-70342C>G
ENST00000370398.6:c.399-70342C>G MANE Select	ENSP00000359425.1:n.399-70342C>G
ENST00000342056.6:c.399-70342C>G	ENSP00000345055.2:n.399-70342C>G
ENST00000355194.8:c.408-70351C>G	ENSP00000347326.4:n.408-70351C>G
ENST00000355635.7:c.408-70351C>G	ENSP00000347853.4:n.408-70351C>G
ENST00000370392.5:c.399-70342C>G	ENSP00000359419.1:n.399-70342C>G
ENST00000370398.5:c.399-70342C>G	ENSP00000359425.1:n.399-70342C>G
ENST00000402622.6:c.408-70351C>G	ENSP00000385501.3:n.408-70351C>G
ENST00000403813.6:c.408-70351C>G	ENSP00000384453.3:n.408-70351C>G
ENST00000414165.6:c.408-70351C>G	ENSP00000409861.3:n.408-70351C>G
ENST00000628967.2:c.399-70342C>G	ENSP00000486187.1:n.399-70342C>G
ENST00000629977.2:c.399-70342C>G	ENSP00000485743.1:n.399-70342C>G
NM_001160130.1:c.399-70342C>G	NP_001153602.1:n.399-70342C>G
NM_001160132.1:c.399-70342C>G	NP_001153604.1:n.399-70342C>G
NM_001160133.1:c.399-70342C>G	NP_001153605.1:n.399-70342C>G
NM_001160134.1:c.399-70342C>G	NP_001153606.1:n.399-70342C>G
NM_019842.3:c.399-70342C>G	NP_062816.2:n.399-70342C>G
XM_011535944.1:c.399-70342C>G	XP_011534246.1:n.399-70342C>G
XM_017011058.1:c.399-70342C>G	XP_016866547.1:n.399-70342C>G
XM_024446492.1:c.399-70342C>G	XP_024302260.1:n.399-70342C>G
XM_024446493.1:c.399-70342C>G	XP_024302261.1:n.399-70342C>G
NM_001160130.2:c.399-70342C>G	NP_001153602.1:n.399-70342C>G
NM_001160132.2:c.399-70342C>G	NP_001153604.1:n.399-70342C>G
NM_001160133.2:c.399-70342C>G	NP_001153605.1:n.399-70342C>G
NM_001160134.2:c.399-70342C>G	NP_001153606.1:n.399-70342C>G
NM_019842.4:c.399-70342C>G MANE Select	NP_062816.2:n.399-70342C>G