Canonical Allele Identifier: CA409639120

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038575C>A (hg19) ; chr20:g.63407222C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407222C>A , CM000682.2:g.63407222C>A	GRCh38
NC_000020.10:g.62038575C>A , CM000682.1:g.62038575C>A	GRCh37
NC_000020.9:g.61509019C>A	NCBI36
NG_009004.1:g.70419G>T
NG_009004.2:g.70419G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2095G>T	ENSP00000516702.1:p.Asp699Tyr
ENST00000359125.7:c.2041G>T MANE Select	ENSP00000352035.2:p.Asp681Tyr
ENST00000637193.1:c.1438G>T	ENSP00000490734.1:p.Asp480Tyr
ENST00000344462.8:c.1948G>T	ENSP00000339611.4:p.Asp650Tyr
ENST00000357249.6:c.1609G>T	ENSP00000349789.3:p.Asp537Tyr
ENST00000359125.6:c.2041G>T	ENSP00000352035.2:p.Asp681Tyr
ENST00000360480.7:c.1957G>T	ENSP00000353668.3:p.Asp653Tyr
ENST00000370224.5:c.2065G>T	ENSP00000359244.2:p.Asp689Tyr
ENST00000625514.2:c.2029G>T	ENSP00000486040.1:p.Asp677Tyr
ENST00000626839.2:c.1987G>T	ENSP00000486706.1:p.Asp663Tyr
ENST00000629241.2:c.1957G>T	ENSP00000487142.1:p.Asp653Tyr
ENST00000629676.2:c.1679+6228G>T	ENSP00000486194.1:n.1679+6228G>T
NM_004518.4:c.1957G>T	NP_004509.2:p.Asp653Tyr
NM_172106.1:c.1987G>T	NP_742104.1:p.Asp663Tyr
NM_172107.2:c.2041G>T	NP_742105.1:p.Asp681Tyr
NM_172108.3:c.1948G>T	NP_742106.1:p.Asp650Tyr
XM_006723787.1:c.2083G>T	XP_006723850.1:p.Asp695Tyr
XM_011528807.1:c.2149G>T	XP_011527109.1:p.Asp717Tyr
XM_011528808.1:c.2146G>T	XP_011527110.1:p.Asp716Tyr
XM_011528809.1:c.2119G>T	XP_011527111.1:p.Asp707Tyr
XM_011528810.1:c.2095G>T	XP_011527112.1:p.Asp699Tyr
XM_011528811.1:c.2065G>T	XP_011527113.1:p.Asp689Tyr
XM_011528812.1:c.2038G>T	XP_011527114.1:p.Asp680Tyr
XM_011528813.1:c.2023G>T	XP_011527115.1:p.Asp675Tyr
XM_011528814.1:c.1630G>T	XP_011527116.1:p.Asp544Tyr
NM_004518.5:c.1957G>T	NP_004509.2:p.Asp653Tyr
NM_172106.2:c.1987G>T	NP_742104.1:p.Asp663Tyr
NM_172107.3:c.2041G>T	NP_742105.1:p.Asp681Tyr
NM_172108.4:c.1948G>T	NP_742106.1:p.Asp650Tyr
XM_011528810.2:c.2095G>T	XP_011527112.1:p.Asp699Tyr
XM_011528811.2:c.2065G>T	XP_011527113.1:p.Asp689Tyr
XM_017027841.2:c.2092G>T	XP_016883330.1:p.Asp698Tyr
XM_017027842.2:c.2029G>T	XP_016883331.1:p.Asp677Tyr
XM_017027843.1:c.2026G>T	XP_016883332.1:p.Asp676Tyr
XM_017027844.2:c.1984G>T	XP_016883333.1:p.Asp662Tyr
XM_017027845.1:c.1057G>T	XP_016883334.1:p.Asp353Tyr
NM_004518.6:c.1957G>T	NP_004509.2:p.Asp653Tyr
NM_172106.3:c.1987G>T	NP_742104.1:p.Asp663Tyr
NM_172107.4:c.2041G>T MANE Select	NP_742105.1:p.Asp681Tyr
NM_172108.5:c.1948G>T	NP_742106.1:p.Asp650Tyr
NM_001382235.1:c.2095G>T	NP_001369164.1:p.Asp699Tyr