Canonical Allele Identifier: CA409639198

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038608A>G (hg19) ; chr20:g.63407255A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407255A>G , CM000682.2:g.63407255A>G	GRCh38
NC_000020.10:g.62038608A>G , CM000682.1:g.62038608A>G	GRCh37
NC_000020.9:g.61509052A>G	NCBI36
NG_009004.1:g.70386T>C
NG_009004.2:g.70386T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2062T>C	ENSP00000516702.1:p.Tyr688His
ENST00000359125.7:c.2008T>C MANE Select	ENSP00000352035.2:p.Tyr670His
ENST00000637193.1:c.1405T>C	ENSP00000490734.1:p.Tyr469His
ENST00000344462.8:c.1915T>C	ENSP00000339611.4:p.Tyr639His
ENST00000357249.6:c.1576T>C	ENSP00000349789.3:p.Tyr526His
ENST00000359125.6:c.2008T>C	ENSP00000352035.2:p.Tyr670His
ENST00000360480.7:c.1924T>C	ENSP00000353668.3:p.Tyr642His
ENST00000370224.5:c.2032T>C	ENSP00000359244.2:p.Tyr678His
ENST00000625514.2:c.1996T>C	ENSP00000486040.1:p.Tyr666His
ENST00000626839.2:c.1954T>C	ENSP00000486706.1:p.Tyr652His
ENST00000629241.2:c.1924T>C	ENSP00000487142.1:p.Tyr642His
ENST00000629676.2:c.1679+6195T>C	ENSP00000486194.1:n.1679+6195T>C
NM_004518.4:c.1924T>C	NP_004509.2:p.Tyr642His
NM_172106.1:c.1954T>C	NP_742104.1:p.Tyr652His
NM_172107.2:c.2008T>C	NP_742105.1:p.Tyr670His
NM_172108.3:c.1915T>C	NP_742106.1:p.Tyr639His
XM_006723787.1:c.2050T>C	XP_006723850.1:p.Tyr684His
XM_011528807.1:c.2116T>C	XP_011527109.1:p.Tyr706His
XM_011528808.1:c.2113T>C	XP_011527110.1:p.Tyr705His
XM_011528809.1:c.2086T>C	XP_011527111.1:p.Tyr696His
XM_011528810.1:c.2062T>C	XP_011527112.1:p.Tyr688His
XM_011528811.1:c.2032T>C	XP_011527113.1:p.Tyr678His
XM_011528812.1:c.2005T>C	XP_011527114.1:p.Tyr669His
XM_011528813.1:c.1990T>C	XP_011527115.1:p.Tyr664His
XM_011528814.1:c.1597T>C	XP_011527116.1:p.Tyr533His
NM_004518.5:c.1924T>C	NP_004509.2:p.Tyr642His
NM_172106.2:c.1954T>C	NP_742104.1:p.Tyr652His
NM_172107.3:c.2008T>C	NP_742105.1:p.Tyr670His
NM_172108.4:c.1915T>C	NP_742106.1:p.Tyr639His
XM_011528810.2:c.2062T>C	XP_011527112.1:p.Tyr688His
XM_011528811.2:c.2032T>C	XP_011527113.1:p.Tyr678His
XM_017027841.2:c.2059T>C	XP_016883330.1:p.Tyr687His
XM_017027842.2:c.1996T>C	XP_016883331.1:p.Tyr666His
XM_017027843.1:c.1993T>C	XP_016883332.1:p.Tyr665His
XM_017027844.2:c.1951T>C	XP_016883333.1:p.Tyr651His
XM_017027845.1:c.1024T>C	XP_016883334.1:p.Tyr342His
NM_004518.6:c.1924T>C	NP_004509.2:p.Tyr642His
NM_172106.3:c.1954T>C	NP_742104.1:p.Tyr652His
NM_172107.4:c.2008T>C MANE Select	NP_742105.1:p.Tyr670His
NM_172108.5:c.1915T>C	NP_742106.1:p.Tyr639His
NM_001382235.1:c.2062T>C	NP_001369164.1:p.Tyr688His