Canonical Allele Identifier: CA233197

Gene: KCNQ4

Linked Data

• ClinVar Variation Id: 156337
• ClinVar RCV Id: RCV000056155 ; RCV000144421
• dbSNP Id: rs137853969
• MyVariant Identifiers: chr1:g.41285571G>C (hg19) ; chr1:g.40819899G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40819899G>C , CM000663.2:g.40819899G>C	GRCh38
NC_000001.10:g.41285571G>C , CM000663.1:g.41285571G>C	GRCh37
NC_000001.9:g.41058158G>C	NCBI36
NG_008139.1:g.40888G>C
NG_008139.2:g.40888G>C
NG_008139.3:g.41113G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000347132.10:c.859G>C MANE Select	ENSP00000262916.6:p.Gly287Arg
ENST00000347132.9:c.859G>C	ENSP00000262916.6:p.Gly287Arg
ENST00000443478.3:c.545G>C
ENST00000506017.1:n.178G>C
ENST00000509682.6:c.859G>C	ENSP00000423756.2:p.Gly287Arg
NM_004700.3:c.859G>C	NP_004691.2:p.Gly287Arg
NM_172163.2:c.859G>C	NP_751895.1:p.Gly287Arg
XM_011542417.1:c.859G>C	XP_011540719.1:p.Gly287Arg
XM_011542418.1:c.859G>C	XP_011540720.1:p.Gly287Arg
XM_011542419.1:c.859G>C	XP_011540721.1:p.Gly287Arg
XM_011542420.1:c.859G>C	XP_011540722.1:p.Gly287Arg
XR_946798.1:n.865G>C
XR_946799.1:n.865G>C
XR_946800.1:n.865G>C
XM_017002792.1:c.-159G>C	XP_016858281.1:n.-159G>C
NM_004700.4:c.859G>C MANE Select	NP_004691.2:p.Gly287Arg
NM_172163.3:c.859G>C	NP_751895.1:p.Gly287Arg