Canonical Allele Identifier: CA1164545349

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40819451C= , CM000663.2:g.40819451C=	GRCh38
NC_000001.10:g.41285123C= , CM000663.1:g.41285123C=	GRCh37
NC_000001.9:g.41057710C=	NCBI36
NG_008139.1:g.40440C=
NG_008139.2:g.40440C=
NG_008139.3:g.40665C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.813C= MANE Select	ENSP00000262916.6:p.Ala271=
ENST00000347132.9:c.813C=	ENSP00000262916.6:p.Ala271=
ENST00000443478.3:c.499C=
ENST00000506017.1:n.132C=
ENST00000509682.6:c.813C=	ENSP00000423756.2:p.Ala271=
NM_004700.3:c.813C=	NP_004691.2:p.Ala271=
NM_172163.2:c.813C=	NP_751895.1:p.Ala271=
XM_011542417.1:c.813C=	XP_011540719.1:p.Ala271=
XM_011542418.1:c.813C=	XP_011540720.1:p.Ala271=
XM_011542419.1:c.813C=	XP_011540721.1:p.Ala271=
XM_011542420.1:c.813C=	XP_011540722.1:p.Ala271=
XR_946798.1:n.819C=
XR_946799.1:n.819C=
XR_946800.1:n.819C=
XM_017002792.1:c.-205C=	XP_016858281.1:n.-205C=
NM_004700.4:c.813C= MANE Select	NP_004691.2:p.Ala271=
NM_172163.3:c.813C=	NP_751895.1:p.Ala271=