Canonical Allele Identifier: CA511339644

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038693C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407340C>G , CM000682.2:g.63407340C>G	GRCh38
NC_000020.10:g.62038693C>G , CM000682.1:g.62038693C>G	GRCh37
NC_000020.9:g.61509137C>G	NCBI36
NG_009004.1:g.70301G>C
NG_009004.2:g.70301G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1977G>C	ENSP00000516702.1:p.Val659=
ENST00000359125.7:c.1923G>C MANE Select	ENSP00000352035.2:p.Val641=
ENST00000637193.1:c.1320G>C	ENSP00000490734.1:p.Val440=
ENST00000637338.1:n.80G>C
ENST00000344462.8:c.1830G>C	ENSP00000339611.4:p.Val610=
ENST00000357249.6:c.1491G>C	ENSP00000349789.3:p.Val497=
ENST00000359125.6:c.1923G>C	ENSP00000352035.2:p.Val641=
ENST00000360480.7:c.1839G>C	ENSP00000353668.3:p.Val613=
ENST00000370224.5:c.1947G>C	ENSP00000359244.2:p.Val649=
ENST00000625514.2:c.1911G>C	ENSP00000486040.1:p.Val637=
ENST00000626839.2:c.1869G>C	ENSP00000486706.1:p.Val623=
ENST00000629241.2:c.1839G>C	ENSP00000487142.1:p.Val613=
ENST00000629676.2:c.1679+6110G>C	ENSP00000486194.1:n.1679+6110G>C
NM_004518.4:c.1839G>C	NP_004509.2:p.Val613=
NM_172106.1:c.1869G>C	NP_742104.1:p.Val623=
NM_172107.2:c.1923G>C	NP_742105.1:p.Val641=
NM_172108.3:c.1830G>C	NP_742106.1:p.Val610=
XM_006723787.1:c.1965G>C	XP_006723850.1:p.Val655=
XM_011528807.1:c.2031G>C	XP_011527109.1:p.Val677=
XM_011528808.1:c.2028G>C	XP_011527110.1:p.Val676=
XM_011528809.1:c.2001G>C	XP_011527111.1:p.Val667=
XM_011528810.1:c.1977G>C	XP_011527112.1:p.Val659=
XM_011528811.1:c.1947G>C	XP_011527113.1:p.Val649=
XM_011528812.1:c.1920G>C	XP_011527114.1:p.Val640=
XM_011528813.1:c.1905G>C	XP_011527115.1:p.Val635=
XM_011528814.1:c.1512G>C	XP_011527116.1:p.Val504=
NM_004518.5:c.1839G>C	NP_004509.2:p.Val613=
NM_172106.2:c.1869G>C	NP_742104.1:p.Val623=
NM_172107.3:c.1923G>C	NP_742105.1:p.Val641=
NM_172108.4:c.1830G>C	NP_742106.1:p.Val610=
XM_011528810.2:c.1977G>C	XP_011527112.1:p.Val659=
XM_011528811.2:c.1947G>C	XP_011527113.1:p.Val649=
XM_017027841.2:c.1974G>C	XP_016883330.1:p.Val658=
XM_017027842.2:c.1911G>C	XP_016883331.1:p.Val637=
XM_017027843.1:c.1908G>C	XP_016883332.1:p.Val636=
XM_017027844.2:c.1866G>C	XP_016883333.1:p.Val622=
XM_017027845.1:c.939G>C	XP_016883334.1:p.Val313=
NM_004518.6:c.1839G>C	NP_004509.2:p.Val613=
NM_172106.3:c.1869G>C	NP_742104.1:p.Val623=
NM_172107.4:c.1923G>C MANE Select	NP_742105.1:p.Val641=
NM_172108.5:c.1830G>C	NP_742106.1:p.Val610=
NM_001382235.1:c.1977G>C	NP_001369164.1:p.Val659=