Canonical Allele Identifier: CA1140511584

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40831156T= , CM000663.2:g.40831156T=	GRCh38
NC_000001.10:g.41296828T= , CM000663.1:g.41296828T=	GRCh37
NC_000001.9:g.41069415T=	NCBI36
NG_008139.1:g.52145T=
NG_008139.2:g.52145T=
NG_008139.3:g.52370T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.1365T= MANE Select	ENSP00000262916.6:p.His455=
ENST00000347132.9:c.1365T=	ENSP00000262916.6:p.His455=
ENST00000443478.3:c.946T=
ENST00000506017.1:n.684T=
ENST00000509682.6:c.1203T=	ENSP00000423756.2:p.His401=
NM_004700.3:c.1365T=	NP_004691.2:p.His455=
NM_172163.2:c.1203T=	NP_751895.1:p.His401=
XR_946798.1:n.1371T=
XR_946799.1:n.1371T=
XR_946800.1:n.1120T=
XM_017002792.1:c.348T=	XP_016858281.1:p.His116=
NM_004700.4:c.1365T= MANE Select	NP_004691.2:p.His455=
NM_172163.3:c.1203T=	NP_751895.1:p.His401=