Canonical Allele Identifier: CA10654832
Gene: KCNQ2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 369744
ClinVar RCV Id: RCV000678119
dbSNP Id: rs1057516079

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63445281C>T , CM000682.2:g.63445281C>T GRCh38
NC_000020.10:g.62076634C>T , CM000682.1:g.62076634C>T GRCh37
NC_000020.9:g.61547078C>T NCBI36
NG_009004.1:g.32360G>A
NG_009004.2:g.32360G>A

Transcript Alleles

HGVS Amino-acid change
NM_004518.4:c.471G>A VV NP_004509.2:p.Trp157Ter
NM_172106.1:c.471G>A VV NP_742104.1:p.Trp157Ter
NM_172107.2:c.471G>A VV NP_742105.1:p.Trp157Ter
NM_172108.3:c.471G>A VV NP_742106.1:p.Trp157Ter
NM_172109.1:c.471G>A VV NP_742107.1:p.Trp157Ter
XM_006723787.1:c.471G>A XP_006723850.1:p.Trp157Ter
XM_011528807.1:c.471G>A XP_011527109.1:p.Trp157Ter
XM_011528808.1:c.471G>A XP_011527110.1:p.Trp157Ter
XM_011528809.1:c.471G>A XP_011527111.1:p.Trp157Ter
XM_011528810.1:c.471G>A XP_011527112.1:p.Trp157Ter
XM_011528811.1:c.471G>A XP_011527113.1:p.Trp157Ter
XM_011528812.1:c.471G>A XP_011527114.1:p.Trp157Ter
XM_011528813.1:c.471G>A XP_011527115.1:p.Trp157Ter
XM_011528814.1:c.-49G>A XP_011527116.1:p.=
XM_011528815.1:c.471G>A XP_011527117.1:p.Trp157Ter
XM_011528816.1:c.471G>A XP_011527118.1:p.Trp157Ter
NM_004518.5:c.471G>A VV
NM_172106.2:c.471G>A VV
NM_172107.3:c.471G>A VV
NM_172108.4:c.471G>A VV
NM_172109.2:c.471G>A VV
XM_011528810.2:c.471G>A
XM_011528811.2:c.471G>A
XM_017027841.2:c.471G>A XP_016883330.1:p.Trp157Ter
XM_017027842.2:c.471G>A XP_016883331.1:p.Trp157Ter
XM_017027843.1:c.402G>A XP_016883332.1:p.Trp134Ter
XM_017027844.2:c.471G>A XP_016883333.1:p.Trp157Ter
ENST00000344425.7:c.471G>A ENSP00000345523.5:p.Trp157Ter
ENST00000344462.8:c.471G>A ENSP00000339611.4:p.Trp157Ter
ENST00000357249.6:n.129G>A ENSP00000349789.3:p.Trp43Ter
ENST00000359125.6:c.471G>A ENSP00000352035.2:p.Trp157Ter
ENST00000360480.7:c.471G>A ENSP00000353668.3:p.Trp157Ter
ENST00000370221.3:n.597G>A
ENST00000370224.5:c.471G>A ENSP00000359244.2:p.Trp157Ter
ENST00000625514.2:c.471G>A ENSP00000486040.1:p.Trp157Ter
ENST00000626313.1:n.313G>A
ENST00000626839.2:c.471G>A ENSP00000486706.1:p.Trp157Ter
ENST00000629241.2:c.471G>A ENSP00000487142.1:p.Trp157Ter
ENST00000629676.2:c.471G>A ENSP00000486194.1:p.Trp157Ter
ENST00000630274.2:n.296G>A