Canonical Allele Identifier: CA1147878300

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40819308C= , CM000663.2:g.40819308C=	GRCh38
NC_000001.10:g.41284980C= , CM000663.1:g.41284980C=	GRCh37
NC_000001.9:g.41057567C=	NCBI36
NG_008139.1:g.40297C=
NG_008139.2:g.40297C=
NG_008139.3:g.40522C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.709-39C= MANE Select	ENSP00000262916.6:n.709-39C=
ENST00000347132.9:c.709-39C=	ENSP00000262916.6:n.709-39C=
ENST00000443478.3:c.395-39C=
ENST00000506017.1:n.28-39C=
ENST00000509682.6:c.709-39C=	ENSP00000423756.2:n.709-39C=
NM_004700.3:c.709-39C=	NP_004691.2:n.709-39C=
NM_172163.2:c.709-39C=	NP_751895.1:n.709-39C=
XM_011542417.1:c.709-39C=	XP_011540719.1:n.709-39C=
XM_011542418.1:c.709-39C=	XP_011540720.1:n.709-39C=
XM_011542419.1:c.709-39C=	XP_011540721.1:n.709-39C=
XM_011542420.1:c.709-39C=	XP_011540722.1:n.709-39C=
XR_946798.1:n.715-39C=
XR_946799.1:n.715-39C=
XR_946800.1:n.715-39C=
XM_017002792.1:c.-309-39C=	XP_016858281.1:n.-309-39C=
NM_004700.4:c.709-39C= MANE Select	NP_004691.2:n.709-39C=
NM_172163.3:c.709-39C=	NP_751895.1:n.709-39C=