Canonical Allele Identifier: CA409646136

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62046274A>C (hg19) ; chr20:g.63414921A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63414921A>C , CM000682.2:g.63414921A>C	GRCh38
NC_000020.10:g.62046274A>C , CM000682.1:g.62046274A>C	GRCh37
NC_000020.9:g.61516718A>C	NCBI36
NG_009004.1:g.62720T>G
NG_009004.2:g.62720T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1453T>G	ENSP00000516702.1:p.Ser485Ala
ENST00000359125.7:c.1507T>G MANE Select	ENSP00000352035.2:p.Ser503Ala
ENST00000637193.1:c.904T>G	ENSP00000490734.1:p.Ser302Ala
ENST00000344462.8:c.1417T>G	ENSP00000339611.4:p.Ser473Ala
ENST00000357249.6:c.1075T>G	ENSP00000349789.3:p.Ser359Ala
ENST00000359125.6:c.1507T>G	ENSP00000352035.2:p.Ser503Ala
ENST00000360480.7:c.1423T>G	ENSP00000353668.3:p.Ser475Ala
ENST00000370224.5:c.1423T>G	ENSP00000359244.2:p.Ser475Ala
ENST00000625514.2:c.1387T>G	ENSP00000486040.1:p.Ser463Ala
ENST00000626839.2:c.1453T>G	ENSP00000486706.1:p.Ser485Ala
ENST00000627221.2:c.567T>G
ENST00000629241.2:c.1423T>G	ENSP00000487142.1:p.Ser475Ala
ENST00000629318.1:c.115T>G	ENSP00000487384.1:p.Ser39Ala
ENST00000629676.2:c.1423T>G	ENSP00000486194.1:p.Ser475Ala
NM_004518.4:c.1423T>G	NP_004509.2:p.Ser475Ala
NM_172106.1:c.1453T>G	NP_742104.1:p.Ser485Ala
NM_172107.2:c.1507T>G	NP_742105.1:p.Ser503Ala
NM_172108.3:c.1417T>G	NP_742106.1:p.Ser473Ala
XM_006723787.1:c.1507T>G	XP_006723850.1:p.Ser503Ala
XM_011528807.1:c.1507T>G	XP_011527109.1:p.Ser503Ala
XM_011528808.1:c.1507T>G	XP_011527110.1:p.Ser503Ala
XM_011528809.1:c.1477T>G	XP_011527111.1:p.Ser493Ala
XM_011528810.1:c.1453T>G	XP_011527112.1:p.Ser485Ala
XM_011528811.1:c.1423T>G	XP_011527113.1:p.Ser475Ala
XM_011528812.1:c.1507T>G	XP_011527114.1:p.Ser503Ala
XM_011528813.1:c.1381T>G	XP_011527115.1:p.Ser461Ala
XM_011528814.1:c.988T>G	XP_011527116.1:p.Ser330Ala
XM_011528815.1:c.1507T>G	XP_011527117.1:p.Ser503Ala
NM_004518.5:c.1423T>G	NP_004509.2:p.Ser475Ala
NM_172106.2:c.1453T>G	NP_742104.1:p.Ser485Ala
NM_172107.3:c.1507T>G	NP_742105.1:p.Ser503Ala
NM_172108.4:c.1417T>G	NP_742106.1:p.Ser473Ala
XM_011528810.2:c.1453T>G	XP_011527112.1:p.Ser485Ala
XM_011528811.2:c.1423T>G	XP_011527113.1:p.Ser475Ala
XM_017027841.2:c.1453T>G	XP_016883330.1:p.Ser485Ala
XM_017027842.2:c.1453T>G	XP_016883331.1:p.Ser485Ala
XM_017027843.1:c.1384T>G	XP_016883332.1:p.Ser462Ala
XM_017027844.2:c.1453T>G	XP_016883333.1:p.Ser485Ala
XM_017027845.1:c.415T>G	XP_016883334.1:p.Ser139Ala
NM_004518.6:c.1423T>G	NP_004509.2:p.Ser475Ala
NM_172106.3:c.1453T>G	NP_742104.1:p.Ser485Ala
NM_172107.4:c.1507T>G MANE Select	NP_742105.1:p.Ser503Ala
NM_172108.5:c.1417T>G	NP_742106.1:p.Ser473Ala
NM_001382235.1:c.1453T>G	NP_001369164.1:p.Ser485Ala