Canonical Allele Identifier: CA182793

Gene: KCNQ4

Linked Data

• ClinVar Variation Id: 178690
• ClinVar RCV Id: RCV000155447 ; RCV000763910
• dbSNP Id: rs727504459
• MyVariant Identifiers: chr1:g.41285139G>A (hg19) ; chr1:g.40819467G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40819467G>A , CM000663.2:g.40819467G>A	GRCh38
NC_000001.10:g.41285139G>A , CM000663.1:g.41285139G>A	GRCh37
NC_000001.9:g.41057726G>A	NCBI36
NG_008139.1:g.40456G>A
NG_008139.2:g.40456G>A
NG_008139.3:g.40681G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000347132.10:c.829G>A MANE Select	ENSP00000262916.6:p.Gly277Arg
ENST00000347132.9:c.829G>A	ENSP00000262916.6:p.Gly277Arg
ENST00000443478.3:c.515G>A
ENST00000506017.1:n.148G>A
ENST00000509682.6:c.829G>A	ENSP00000423756.2:p.Gly277Arg
NM_004700.3:c.829G>A	NP_004691.2:p.Gly277Arg
NM_172163.2:c.829G>A	NP_751895.1:p.Gly277Arg
XM_011542417.1:c.829G>A	XP_011540719.1:p.Gly277Arg
XM_011542418.1:c.829G>A	XP_011540720.1:p.Gly277Arg
XM_011542419.1:c.829G>A	XP_011540721.1:p.Gly277Arg
XM_011542420.1:c.829G>A	XP_011540722.1:p.Gly277Arg
XR_946798.1:n.835G>A
XR_946799.1:n.835G>A
XR_946800.1:n.835G>A
XM_017002792.1:c.-189G>A	XP_016858281.1:n.-189G>A
NM_004700.4:c.829G>A MANE Select	NP_004691.2:p.Gly277Arg
NM_172163.3:c.829G>A	NP_751895.1:p.Gly277Arg