Canonical Allele Identifier: CA1164545332

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40819392G= , CM000663.2:g.40819392G=	GRCh38
NC_000001.10:g.41285064G= , CM000663.1:g.41285064G=	GRCh37
NC_000001.9:g.41057651G=	NCBI36
NG_008139.1:g.40381G=
NG_008139.2:g.40381G=
NG_008139.3:g.40606G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.754G= MANE Select	ENSP00000262916.6:p.Ala252=
ENST00000347132.9:c.754G=	ENSP00000262916.6:p.Ala252=
ENST00000443478.3:c.440G=
ENST00000506017.1:n.73G=
ENST00000509682.6:c.754G=	ENSP00000423756.2:p.Ala252=
NM_004700.3:c.754G=	NP_004691.2:p.Ala252=
NM_172163.2:c.754G=	NP_751895.1:p.Ala252=
XM_011542417.1:c.754G=	XP_011540719.1:p.Ala252=
XM_011542418.1:c.754G=	XP_011540720.1:p.Ala252=
XM_011542419.1:c.754G=	XP_011540721.1:p.Ala252=
XM_011542420.1:c.754G=	XP_011540722.1:p.Ala252=
XR_946798.1:n.760G=
XR_946799.1:n.760G=
XR_946800.1:n.760G=
XM_017002792.1:c.-264G=	XP_016858281.1:n.-264G=
NM_004700.4:c.754G= MANE Select	NP_004691.2:p.Ala252=
NM_172163.3:c.754G=	NP_751895.1:p.Ala252=