Canonical Allele Identifier: CA794535

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40818152C>G , CM000663.2:g.40818152C>G	GRCh38
NC_000001.10:g.41283824C>G , CM000663.1:g.41283824C>G	GRCh37
NC_000001.9:g.41056411C>G	NCBI36
NG_008139.1:g.39141C>G
NG_008139.2:g.39141C>G
NG_008139.3:g.39366C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004700.4:c.406-12C>G MANE Select	NP_004691.2:n.406-12C>G
ENST00000347132.10:c.406-12C>G MANE Select	ENSP00000262916.6:n.406-12C>G
NM_004700.3:c.406-12C>G	NP_004691.2:n.406-12C>G
NM_172163.2:c.406-12C>G	NP_751895.1:n.406-12C>G
NM_172163.3:c.406-12C>G	NP_751895.1:n.406-12C>G
ENST00000347132.9:c.406-12C>G	ENSP00000262916.6:n.406-12C>G
ENST00000443478.3:c.92-12C>G
ENST00000509682.6:c.406-12C>G	ENSP00000423756.2:n.406-12C>G
XM_011542417.1:c.406-12C>G	XP_011540719.1:n.406-12C>G
XM_011542418.1:c.406-12C>G	XP_011540720.1:n.406-12C>G
XM_011542419.1:c.406-12C>G	XP_011540721.1:n.406-12C>G
XM_011542420.1:c.406-12C>G	XP_011540722.1:n.406-12C>G
XR_946798.1:n.412-12C>G
XR_946799.1:n.412-12C>G
XR_946800.1:n.412-12C>G