Canonical Allele Identifier: CA1164550134

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40831079G= , CM000663.2:g.40831079G=	GRCh38
NC_000001.10:g.41296751G= , CM000663.1:g.41296751G=	GRCh37
NC_000001.9:g.41069338G=	NCBI36
NG_008139.1:g.52068G=
NG_008139.2:g.52068G=
NG_008139.3:g.52293G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000347132.10:c.1293-5G= MANE Select	ENSP00000262916.6:n.1293-5G=
ENST00000347132.9:c.1293-5G=	ENSP00000262916.6:n.1293-5G=
ENST00000443478.3:c.874-5G=
ENST00000506017.1:n.612-5G=
ENST00000509682.6:c.1131-5G=	ENSP00000423756.2:n.1131-5G=
NM_004700.3:c.1293-5G=	NP_004691.2:n.1293-5G=
NM_172163.2:c.1131-5G=	NP_751895.1:n.1131-5G=
XR_946798.1:n.1299-5G=
XR_946799.1:n.1299-5G=
XR_946800.1:n.1048-5G=
XM_017002792.1:c.276-5G=	XP_016858281.1:n.276-5G=
NM_004700.4:c.1293-5G= MANE Select	NP_004691.2:n.1293-5G=
NM_172163.3:c.1131-5G=	NP_751895.1:n.1131-5G=