Canonical Allele Identifier: CA1164549932

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40830771T= , CM000663.2:g.40830771T=	GRCh38
NC_000001.10:g.41296443T= , CM000663.1:g.41296443T=	GRCh37
NC_000001.9:g.41069030T=	NCBI36
NG_008139.1:g.51760T=
NG_008139.2:g.51760T=
NG_008139.3:g.51985T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.1293-313T= MANE Select	ENSP00000262916.6:n.1293-313T=
ENST00000347132.9:c.1293-313T=	ENSP00000262916.6:n.1293-313T=
ENST00000443478.3:c.874-313T=
ENST00000506017.1:n.612-313T=
ENST00000509682.6:c.1131-313T=	ENSP00000423756.2:n.1131-313T=
NM_004700.3:c.1293-313T=	NP_004691.2:n.1293-313T=
NM_172163.2:c.1131-313T=	NP_751895.1:n.1131-313T=
XM_011542418.1:c.1289T=	XP_011540720.1:p.Val430=
XR_946798.1:n.1299-313T=
XR_946799.1:n.1299-313T=
XR_946800.1:n.1048-313T=
XM_017002792.1:c.276-313T=	XP_016858281.1:n.276-313T=
NM_004700.4:c.1293-313T= MANE Select	NP_004691.2:n.1293-313T=
NM_172163.3:c.1131-313T=	NP_751895.1:n.1131-313T=