Canonical Allele Identifier: CA339885312

Gene: KCNQ4

Linked Data

• ClinVar Variation Id: 1800917
• ClinVar RCV Id: RCV002462514
• MyVariant Identifiers: chr1:g.41249996C>A (hg19) ; chr1:g.40784324C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40784324C>A , CM000663.2:g.40784324C>A	GRCh38
NC_000001.10:g.41249996C>A , CM000663.1:g.41249996C>A	GRCh37
NC_000001.9:g.41022583C>A	NCBI36
NG_008139.1:g.5313C>A
NG_008139.2:g.5313C>A
NG_008139.3:g.5538C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.231C>A MANE Select	ENSP00000262916.6:p.His77Gln
ENST00000347132.9:c.231C>A	ENSP00000262916.6:p.His77Gln
ENST00000509682.6:c.231C>A	ENSP00000423756.2:p.His77Gln
NM_004700.3:c.231C>A	NP_004691.2:p.His77Gln
NM_172163.2:c.231C>A	NP_751895.1:p.His77Gln
XM_011542417.1:c.231C>A	XP_011540719.1:p.His77Gln
XM_011542418.1:c.231C>A	XP_011540720.1:p.His77Gln
XM_011542419.1:c.231C>A	XP_011540721.1:p.His77Gln
XM_011542420.1:c.231C>A	XP_011540722.1:p.His77Gln
XR_946798.1:n.237C>A
XR_946799.1:n.237C>A
XR_946800.1:n.237C>A
NM_004700.4:c.231C>A MANE Select	NP_004691.2:p.His77Gln
NM_172163.3:c.231C>A	NP_751895.1:p.His77Gln