Canonical Allele Identifier: CA21082986

Gene: KCNQ4

Linked Data

• dbSNP Id: rs923241386
• MyVariant Identifiers: chr1:g.41296459T>C (hg19) ; chr1:g.40830787T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40830787T>C , CM000663.2:g.40830787T>C	GRCh38
NC_000001.10:g.41296459T>C , CM000663.1:g.41296459T>C	GRCh37
NC_000001.9:g.41069046T>C	NCBI36
NG_008139.1:g.51776T>C
NG_008139.2:g.51776T>C
NG_008139.3:g.52001T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.1293-297T>C MANE Select	ENSP00000262916.6:n.1293-297T>C
ENST00000347132.9:c.1293-297T>C	ENSP00000262916.6:n.1293-297T>C
ENST00000443478.3:c.874-297T>C
ENST00000506017.1:n.612-297T>C
ENST00000509682.6:c.1131-297T>C	ENSP00000423756.2:n.1131-297T>C
NM_004700.3:c.1293-297T>C	NP_004691.2:n.1293-297T>C
NM_172163.2:c.1131-297T>C	NP_751895.1:n.1131-297T>C
XM_011542418.1:c.1305T>C	XP_011540720.1:p.Asp435=
XR_946798.1:n.1299-297T>C
XR_946799.1:n.1299-297T>C
XR_946800.1:n.1048-297T>C
XM_017002792.1:c.276-297T>C	XP_016858281.1:n.276-297T>C
NM_004700.4:c.1293-297T>C MANE Select	NP_004691.2:n.1293-297T>C
NM_172163.3:c.1131-297T>C	NP_751895.1:n.1131-297T>C