Canonical Allele Identifier: CA1164553096

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40838383G= , CM000663.2:g.40838383G=	GRCh38
NC_000001.10:g.41304055G= , CM000663.1:g.41304055G=	GRCh37
NC_000001.9:g.41076642G=	NCBI36
NG_008139.1:g.59372G=
NG_008139.2:g.59372G=
NG_008139.3:g.59597G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.1948G= MANE Select	ENSP00000262916.6:p.Ala650=
ENST00000347132.9:c.1948G=	ENSP00000262916.6:p.Ala650=
ENST00000443478.3:c.1529G=
ENST00000506017.1:n.1267G=
ENST00000509682.6:c.1786G=	ENSP00000423756.2:p.Ala596=
NM_004700.3:c.1948G=	NP_004691.2:p.Ala650=
NM_172163.2:c.1786G=	NP_751895.1:p.Ala596=
XM_017002792.1:c.931G=	XP_016858281.1:p.Ala311=
NM_004700.4:c.1948G= MANE Select	NP_004691.2:p.Ala650=
NM_172163.3:c.1786G=	NP_751895.1:p.Ala596=