Canonical Allele Identifier: CA1164551681

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40835015A= , CM000663.2:g.40835015A=	GRCh38
NC_000001.10:g.41300687A= , CM000663.1:g.41300687A=	GRCh37
NC_000001.9:g.41073274A=	NCBI36
NG_008139.1:g.56004A=
NG_008139.2:g.56004A=
NG_008139.3:g.56229A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.1662A= MANE Select	ENSP00000262916.6:p.Arg554=
ENST00000347132.9:c.1662A=	ENSP00000262916.6:p.Arg554=
ENST00000443478.3:c.1243A=
ENST00000506017.1:n.981A=
ENST00000509682.6:c.1500A=	ENSP00000423756.2:p.Arg500=
NM_004700.3:c.1662A=	NP_004691.2:p.Arg554=
NM_172163.2:c.1500A=	NP_751895.1:p.Arg500=
XR_946798.1:n.1684A=
XR_946799.1:n.1684A=
XR_946800.1:n.1417A=
XM_017002792.1:c.645A=	XP_016858281.1:p.Arg215=
NM_004700.4:c.1662A= MANE Select	NP_004691.2:p.Arg554=
NM_172163.3:c.1500A=	NP_751895.1:p.Arg500=