Canonical Allele Identifier: CA409638969

Gene: KCNQ2

Linked Data

• ClinVar Variation Id: 1311778
• ClinVar RCV Id: RCV001752761
• dbSNP Id: rs1242898915
• gnomAD v2: 20-62038506-G-A
• gnomAD v4: 20-63407153-G-A
• MyVariant Identifiers: chr20:g.62038506G>A (hg19) ; chr20:g.63407153G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407153G>A , CM000682.2:g.63407153G>A	GRCh38
NC_000020.10:g.62038506G>A , CM000682.1:g.62038506G>A	GRCh37
NC_000020.9:g.61508950G>A	NCBI36
NG_009004.1:g.70488C>T
NG_009004.2:g.70488C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2164C>T	ENSP00000516702.1:p.Pro722Ser
ENST00000359125.7:c.2110C>T MANE Select	ENSP00000352035.2:p.Pro704Ser
ENST00000637193.1:c.1507C>T	ENSP00000490734.1:p.Pro503Ser
ENST00000344462.8:c.2017C>T	ENSP00000339611.4:p.Pro673Ser
ENST00000357249.6:c.1678C>T	ENSP00000349789.3:p.Pro560Ser
ENST00000359125.6:c.2110C>T	ENSP00000352035.2:p.Pro704Ser
ENST00000360480.7:c.2026C>T	ENSP00000353668.3:p.Pro676Ser
ENST00000370224.5:c.2134C>T	ENSP00000359244.2:p.Pro712Ser
ENST00000625514.2:c.2098C>T	ENSP00000486040.1:p.Pro700Ser
ENST00000626839.2:c.2056C>T	ENSP00000486706.1:p.Pro686Ser
ENST00000629241.2:c.2026C>T	ENSP00000487142.1:p.Pro676Ser
ENST00000629676.2:c.1679+6297C>T	ENSP00000486194.1:n.1679+6297C>T
NM_004518.4:c.2026C>T	NP_004509.2:p.Pro676Ser
NM_172106.1:c.2056C>T	NP_742104.1:p.Pro686Ser
NM_172107.2:c.2110C>T	NP_742105.1:p.Pro704Ser
NM_172108.3:c.2017C>T	NP_742106.1:p.Pro673Ser
XM_006723787.1:c.2152C>T	XP_006723850.1:p.Pro718Ser
XM_011528807.1:c.2218C>T	XP_011527109.1:p.Pro740Ser
XM_011528808.1:c.2215C>T	XP_011527110.1:p.Pro739Ser
XM_011528809.1:c.2188C>T	XP_011527111.1:p.Pro730Ser
XM_011528810.1:c.2164C>T	XP_011527112.1:p.Pro722Ser
XM_011528811.1:c.2134C>T	XP_011527113.1:p.Pro712Ser
XM_011528812.1:c.2107C>T	XP_011527114.1:p.Pro703Ser
XM_011528813.1:c.2092C>T	XP_011527115.1:p.Pro698Ser
XM_011528814.1:c.1699C>T	XP_011527116.1:p.Pro567Ser
NM_004518.5:c.2026C>T	NP_004509.2:p.Pro676Ser
NM_172106.2:c.2056C>T	NP_742104.1:p.Pro686Ser
NM_172107.3:c.2110C>T	NP_742105.1:p.Pro704Ser
NM_172108.4:c.2017C>T	NP_742106.1:p.Pro673Ser
XM_011528810.2:c.2164C>T	XP_011527112.1:p.Pro722Ser
XM_011528811.2:c.2134C>T	XP_011527113.1:p.Pro712Ser
XM_017027841.2:c.2161C>T	XP_016883330.1:p.Pro721Ser
XM_017027842.2:c.2098C>T	XP_016883331.1:p.Pro700Ser
XM_017027843.1:c.2095C>T	XP_016883332.1:p.Pro699Ser
XM_017027844.2:c.2053C>T	XP_016883333.1:p.Pro685Ser
XM_017027845.1:c.1126C>T	XP_016883334.1:p.Pro376Ser
NM_004518.6:c.2026C>T	NP_004509.2:p.Pro676Ser
NM_172106.3:c.2056C>T	NP_742104.1:p.Pro686Ser
NM_172107.4:c.2110C>T MANE Select	NP_742105.1:p.Pro704Ser
NM_172108.5:c.2017C>T	NP_742106.1:p.Pro673Ser
NM_001382235.1:c.2164C>T	NP_001369164.1:p.Pro722Ser