Canonical Allele Identifier: CA511339563

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038663G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407310G>C , CM000682.2:g.63407310G>C	GRCh38
NC_000020.10:g.62038663G>C , CM000682.1:g.62038663G>C	GRCh37
NC_000020.9:g.61509107G>C	NCBI36
NG_009004.1:g.70331C>G
NG_009004.2:g.70331C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2007C>G	ENSP00000516702.1:p.Pro669=
ENST00000359125.7:c.1953C>G MANE Select	ENSP00000352035.2:p.Pro651=
ENST00000637193.1:c.1350C>G	ENSP00000490734.1:p.Pro450=
ENST00000344462.8:c.1860C>G	ENSP00000339611.4:p.Pro620=
ENST00000357249.6:c.1521C>G	ENSP00000349789.3:p.Pro507=
ENST00000359125.6:c.1953C>G	ENSP00000352035.2:p.Pro651=
ENST00000360480.7:c.1869C>G	ENSP00000353668.3:p.Pro623=
ENST00000370224.5:c.1977C>G	ENSP00000359244.2:p.Pro659=
ENST00000625514.2:c.1941C>G	ENSP00000486040.1:p.Pro647=
ENST00000626839.2:c.1899C>G	ENSP00000486706.1:p.Pro633=
ENST00000629241.2:c.1869C>G	ENSP00000487142.1:p.Pro623=
ENST00000629676.2:c.1679+6140C>G	ENSP00000486194.1:n.1679+6140C>G
NM_004518.4:c.1869C>G	NP_004509.2:p.Pro623=
NM_172106.1:c.1899C>G	NP_742104.1:p.Pro633=
NM_172107.2:c.1953C>G	NP_742105.1:p.Pro651=
NM_172108.3:c.1860C>G	NP_742106.1:p.Pro620=
XM_006723787.1:c.1995C>G	XP_006723850.1:p.Pro665=
XM_011528807.1:c.2061C>G	XP_011527109.1:p.Pro687=
XM_011528808.1:c.2058C>G	XP_011527110.1:p.Pro686=
XM_011528809.1:c.2031C>G	XP_011527111.1:p.Pro677=
XM_011528810.1:c.2007C>G	XP_011527112.1:p.Pro669=
XM_011528811.1:c.1977C>G	XP_011527113.1:p.Pro659=
XM_011528812.1:c.1950C>G	XP_011527114.1:p.Pro650=
XM_011528813.1:c.1935C>G	XP_011527115.1:p.Pro645=
XM_011528814.1:c.1542C>G	XP_011527116.1:p.Pro514=
NM_004518.5:c.1869C>G	NP_004509.2:p.Pro623=
NM_172106.2:c.1899C>G	NP_742104.1:p.Pro633=
NM_172107.3:c.1953C>G	NP_742105.1:p.Pro651=
NM_172108.4:c.1860C>G	NP_742106.1:p.Pro620=
XM_011528810.2:c.2007C>G	XP_011527112.1:p.Pro669=
XM_011528811.2:c.1977C>G	XP_011527113.1:p.Pro659=
XM_017027841.2:c.2004C>G	XP_016883330.1:p.Pro668=
XM_017027842.2:c.1941C>G	XP_016883331.1:p.Pro647=
XM_017027843.1:c.1938C>G	XP_016883332.1:p.Pro646=
XM_017027844.2:c.1896C>G	XP_016883333.1:p.Pro632=
XM_017027845.1:c.969C>G	XP_016883334.1:p.Pro323=
NM_004518.6:c.1869C>G	NP_004509.2:p.Pro623=
NM_172106.3:c.1899C>G	NP_742104.1:p.Pro633=
NM_172107.4:c.1953C>G MANE Select	NP_742105.1:p.Pro651=
NM_172108.5:c.1860C>G	NP_742106.1:p.Pro620=
NM_001382235.1:c.2007C>G	NP_001369164.1:p.Pro669=