Canonical Allele Identifier: CA409637570

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038263C>A (hg19) ; chr20:g.63406910C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406910C>A , CM000682.2:g.63406910C>A	GRCh38
NC_000020.10:g.62038263C>A , CM000682.1:g.62038263C>A	GRCh37
NC_000020.9:g.61508707C>A	NCBI36
NG_009004.1:g.70731G>T
NG_009004.2:g.70731G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2407G>T	ENSP00000516702.1:p.Asp803Tyr
ENST00000359125.7:c.2353G>T MANE Select	ENSP00000352035.2:p.Asp785Tyr
ENST00000637193.1:c.1750G>T	ENSP00000490734.1:p.Asp584Tyr
ENST00000344462.8:c.2260G>T	ENSP00000339611.4:p.Asp754Tyr
ENST00000357249.6:c.1921G>T	ENSP00000349789.3:p.Asp641Tyr
ENST00000359125.6:c.2353G>T	ENSP00000352035.2:p.Asp785Tyr
ENST00000360480.7:c.2269G>T	ENSP00000353668.3:p.Asp757Tyr
ENST00000370224.5:c.2241+136G>T	ENSP00000359244.2:n.2241+136G>T
ENST00000625514.2:c.2205+136G>T	ENSP00000486040.1:n.2205+136G>T
ENST00000626839.2:c.2299G>T	ENSP00000486706.1:p.Asp767Tyr
ENST00000629241.2:c.2133+136G>T	ENSP00000487142.1:n.2133+136G>T
ENST00000629676.2:c.1680-6067G>T	ENSP00000486194.1:n.1680-6067G>T
NM_004518.4:c.2269G>T	NP_004509.2:p.Asp757Tyr
NM_172106.1:c.2299G>T	NP_742104.1:p.Asp767Tyr
NM_172107.2:c.2353G>T	NP_742105.1:p.Asp785Tyr
NM_172108.3:c.2260G>T	NP_742106.1:p.Asp754Tyr
XM_006723787.1:c.2395G>T	XP_006723850.1:p.Asp799Tyr
XM_011528807.1:c.2461G>T	XP_011527109.1:p.Asp821Tyr
XM_011528808.1:c.2458G>T	XP_011527110.1:p.Asp820Tyr
XM_011528809.1:c.2431G>T	XP_011527111.1:p.Asp811Tyr
XM_011528810.1:c.2407G>T	XP_011527112.1:p.Asp803Tyr
XM_011528811.1:c.2377G>T	XP_011527113.1:p.Asp793Tyr
XM_011528812.1:c.2350G>T	XP_011527114.1:p.Asp784Tyr
XM_011528813.1:c.2335G>T	XP_011527115.1:p.Asp779Tyr
XM_011528814.1:c.1942G>T	XP_011527116.1:p.Asp648Tyr
NM_004518.5:c.2269G>T	NP_004509.2:p.Asp757Tyr
NM_172106.2:c.2299G>T	NP_742104.1:p.Asp767Tyr
NM_172107.3:c.2353G>T	NP_742105.1:p.Asp785Tyr
NM_172108.4:c.2260G>T	NP_742106.1:p.Asp754Tyr
XM_011528810.2:c.2407G>T	XP_011527112.1:p.Asp803Tyr
XM_011528811.2:c.2377G>T	XP_011527113.1:p.Asp793Tyr
XM_017027841.2:c.2404G>T	XP_016883330.1:p.Asp802Tyr
XM_017027842.2:c.2341G>T	XP_016883331.1:p.Asp781Tyr
XM_017027843.1:c.2338G>T	XP_016883332.1:p.Asp780Tyr
XM_017027844.2:c.2296G>T	XP_016883333.1:p.Asp766Tyr
XM_017027845.1:c.1369G>T	XP_016883334.1:p.Asp457Tyr
NM_004518.6:c.2269G>T	NP_004509.2:p.Asp757Tyr
NM_172106.3:c.2299G>T	NP_742104.1:p.Asp767Tyr
NM_172107.4:c.2353G>T MANE Select	NP_742105.1:p.Asp785Tyr
NM_172108.5:c.2260G>T	NP_742106.1:p.Asp754Tyr
NM_001382235.1:c.2407G>T	NP_001369164.1:p.Asp803Tyr