Canonical Allele Identifier: CA1164549905

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40830725T= , CM000663.2:g.40830725T=	GRCh38
NC_000001.10:g.41296397T= , CM000663.1:g.41296397T=	GRCh37
NC_000001.9:g.41068984T=	NCBI36
NG_008139.1:g.51714T=
NG_008139.2:g.51714T=
NG_008139.3:g.51939T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.1293-359T= MANE Select	ENSP00000262916.6:n.1293-359T=
ENST00000347132.9:c.1293-359T=	ENSP00000262916.6:n.1293-359T=
ENST00000443478.3:c.874-359T=
ENST00000506017.1:n.612-359T=
ENST00000509682.6:c.1131-359T=	ENSP00000423756.2:n.1131-359T=
NM_004700.3:c.1293-359T=	NP_004691.2:n.1293-359T=
NM_172163.2:c.1131-359T=	NP_751895.1:n.1131-359T=
XM_011542418.1:c.1243T=	XP_011540720.1:p.Cys415=
XR_946798.1:n.1299-359T=
XR_946799.1:n.1299-359T=
XR_946800.1:n.1048-359T=
XM_017002792.1:c.276-359T=	XP_016858281.1:n.276-359T=
NM_004700.4:c.1293-359T= MANE Select	NP_004691.2:n.1293-359T=
NM_172163.3:c.1131-359T=	NP_751895.1:n.1131-359T=