Canonical Allele Identifier: CA409637694

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038281C>A (hg19) ; chr20:g.63406928C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406928C>A , CM000682.2:g.63406928C>A	GRCh38
NC_000020.10:g.62038281C>A , CM000682.1:g.62038281C>A	GRCh37
NC_000020.9:g.61508725C>A	NCBI36
NG_009004.1:g.70713G>T
NG_009004.2:g.70713G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2389G>T	ENSP00000516702.1:p.Gly797Trp
ENST00000359125.7:c.2335G>T MANE Select	ENSP00000352035.2:p.Gly779Trp
ENST00000637193.1:c.1732G>T	ENSP00000490734.1:p.Gly578Trp
ENST00000344462.8:c.2242G>T	ENSP00000339611.4:p.Gly748Trp
ENST00000357249.6:c.1903G>T	ENSP00000349789.3:p.Gly635Trp
ENST00000359125.6:c.2335G>T	ENSP00000352035.2:p.Gly779Trp
ENST00000360480.7:c.2251G>T	ENSP00000353668.3:p.Gly751Trp
ENST00000370224.5:c.2241+118G>T	ENSP00000359244.2:n.2241+118G>T
ENST00000625514.2:c.2205+118G>T	ENSP00000486040.1:n.2205+118G>T
ENST00000626839.2:c.2281G>T	ENSP00000486706.1:p.Gly761Trp
ENST00000629241.2:c.2133+118G>T	ENSP00000487142.1:n.2133+118G>T
ENST00000629676.2:c.1680-6085G>T	ENSP00000486194.1:n.1680-6085G>T
NM_004518.4:c.2251G>T	NP_004509.2:p.Gly751Trp
NM_172106.1:c.2281G>T	NP_742104.1:p.Gly761Trp
NM_172107.2:c.2335G>T	NP_742105.1:p.Gly779Trp
NM_172108.3:c.2242G>T	NP_742106.1:p.Gly748Trp
XM_006723787.1:c.2377G>T	XP_006723850.1:p.Gly793Trp
XM_011528807.1:c.2443G>T	XP_011527109.1:p.Gly815Trp
XM_011528808.1:c.2440G>T	XP_011527110.1:p.Gly814Trp
XM_011528809.1:c.2413G>T	XP_011527111.1:p.Gly805Trp
XM_011528810.1:c.2389G>T	XP_011527112.1:p.Gly797Trp
XM_011528811.1:c.2359G>T	XP_011527113.1:p.Gly787Trp
XM_011528812.1:c.2332G>T	XP_011527114.1:p.Gly778Trp
XM_011528813.1:c.2317G>T	XP_011527115.1:p.Gly773Trp
XM_011528814.1:c.1924G>T	XP_011527116.1:p.Gly642Trp
NM_004518.5:c.2251G>T	NP_004509.2:p.Gly751Trp
NM_172106.2:c.2281G>T	NP_742104.1:p.Gly761Trp
NM_172107.3:c.2335G>T	NP_742105.1:p.Gly779Trp
NM_172108.4:c.2242G>T	NP_742106.1:p.Gly748Trp
XM_011528810.2:c.2389G>T	XP_011527112.1:p.Gly797Trp
XM_011528811.2:c.2359G>T	XP_011527113.1:p.Gly787Trp
XM_017027841.2:c.2386G>T	XP_016883330.1:p.Gly796Trp
XM_017027842.2:c.2323G>T	XP_016883331.1:p.Gly775Trp
XM_017027843.1:c.2320G>T	XP_016883332.1:p.Gly774Trp
XM_017027844.2:c.2278G>T	XP_016883333.1:p.Gly760Trp
XM_017027845.1:c.1351G>T	XP_016883334.1:p.Gly451Trp
NM_004518.6:c.2251G>T	NP_004509.2:p.Gly751Trp
NM_172106.3:c.2281G>T	NP_742104.1:p.Gly761Trp
NM_172107.4:c.2335G>T MANE Select	NP_742105.1:p.Gly779Trp
NM_172108.5:c.2242G>T	NP_742106.1:p.Gly748Trp
NM_001382235.1:c.2389G>T	NP_001369164.1:p.Gly797Trp