Canonical Allele Identifier: CA1164545341

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40819434G= , CM000663.2:g.40819434G=	GRCh38
NC_000001.10:g.41285106G= , CM000663.1:g.41285106G=	GRCh37
NC_000001.9:g.41057693G=	NCBI36
NG_008139.1:g.40423G=
NG_008139.2:g.40423G=
NG_008139.3:g.40648G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.796G= MANE Select	ENSP00000262916.6:p.Asp266=
ENST00000347132.9:c.796G=	ENSP00000262916.6:p.Asp266=
ENST00000443478.3:c.482G=
ENST00000506017.1:n.115G=
ENST00000509682.6:c.796G=	ENSP00000423756.2:p.Asp266=
NM_004700.3:c.796G=	NP_004691.2:p.Asp266=
NM_172163.2:c.796G=	NP_751895.1:p.Asp266=
XM_011542417.1:c.796G=	XP_011540719.1:p.Asp266=
XM_011542418.1:c.796G=	XP_011540720.1:p.Asp266=
XM_011542419.1:c.796G=	XP_011540721.1:p.Asp266=
XM_011542420.1:c.796G=	XP_011540722.1:p.Asp266=
XR_946798.1:n.802G=
XR_946799.1:n.802G=
XR_946800.1:n.802G=
XM_017002792.1:c.-222G=	XP_016858281.1:n.-222G=
NM_004700.4:c.796G= MANE Select	NP_004691.2:p.Asp266=
NM_172163.3:c.796G=	NP_751895.1:p.Asp266=