Canonical Allele Identifier: CA339891520

Gene: KCNQ4

Linked Data

• MyVariant Identifiers: chr1:g.41304153G>T (hg19) ; chr1:g.40838481G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40838481G>T , CM000663.2:g.40838481G>T	GRCh38
NC_000001.10:g.41304153G>T , CM000663.1:g.41304153G>T	GRCh37
NC_000001.9:g.41076740G>T	NCBI36
NG_008139.1:g.59470G>T
NG_008139.2:g.59470G>T
NG_008139.3:g.59695G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.2046G>T MANE Select	ENSP00000262916.6:p.Gln682His
ENST00000347132.9:c.2046G>T	ENSP00000262916.6:p.Gln682His
ENST00000443478.3:c.1627G>T
ENST00000506017.1:n.1365G>T
ENST00000509682.6:c.1884G>T	ENSP00000423756.2:p.Gln628His
NM_004700.3:c.2046G>T	NP_004691.2:p.Gln682His
NM_172163.2:c.1884G>T	NP_751895.1:p.Gln628His
XM_017002792.1:c.1029G>T	XP_016858281.1:p.Gln343His
NM_004700.4:c.2046G>T MANE Select	NP_004691.2:p.Gln682His
NM_172163.3:c.1884G>T	NP_751895.1:p.Gln628His