Canonical Allele Identifier: CA2374774264

Gene: KCNQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406835A= , CM000682.2:g.63406835A=	GRCh38
NC_000020.10:g.62038188A= , CM000682.1:g.62038188A=	GRCh37
NC_000020.9:g.61508632A=	NCBI36
NG_009004.1:g.70806T=
NG_009004.2:g.70806T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2482T=	ENSP00000516702.1:p.Ser828=
ENST00000359125.7:c.2428T= MANE Select	ENSP00000352035.2:p.Ser810=
ENST00000637193.1:c.1825T=	ENSP00000490734.1:p.Ser609=
ENST00000344462.8:c.2335T=	ENSP00000339611.4:p.Ser779=
ENST00000357249.6:c.1996T=	ENSP00000349789.3:p.Ser666=
ENST00000359125.6:c.2428T=	ENSP00000352035.2:p.Ser810=
ENST00000360480.7:c.2344T=	ENSP00000353668.3:p.Ser782=
ENST00000370224.5:c.2241+211T=	ENSP00000359244.2:n.2241+211T=
ENST00000625514.2:c.2205+211T=	ENSP00000486040.1:n.2205+211T=
ENST00000626839.2:c.2374T=	ENSP00000486706.1:p.Ser792=
ENST00000629241.2:c.2133+211T=	ENSP00000487142.1:n.2133+211T=
ENST00000629676.2:c.1680-5992T=	ENSP00000486194.1:n.1680-5992T=
NM_004518.4:c.2344T=	NP_004509.2:p.Ser782=
NM_172106.1:c.2374T=	NP_742104.1:p.Ser792=
NM_172107.2:c.2428T=	NP_742105.1:p.Ser810=
NM_172108.3:c.2335T=	NP_742106.1:p.Ser779=
XM_006723787.1:c.2470T=	XP_006723850.1:p.Ser824=
XM_011528807.1:c.2536T=	XP_011527109.1:p.Ser846=
XM_011528808.1:c.2533T=	XP_011527110.1:p.Ser845=
XM_011528809.1:c.2506T=	XP_011527111.1:p.Ser836=
XM_011528810.1:c.2482T=	XP_011527112.1:p.Ser828=
XM_011528811.1:c.2452T=	XP_011527113.1:p.Ser818=
XM_011528812.1:c.2425T=	XP_011527114.1:p.Ser809=
XM_011528813.1:c.2410T=	XP_011527115.1:p.Ser804=
XM_011528814.1:c.2017T=	XP_011527116.1:p.Ser673=
NM_004518.5:c.2344T=	NP_004509.2:p.Ser782=
NM_172106.2:c.2374T=	NP_742104.1:p.Ser792=
NM_172107.3:c.2428T=	NP_742105.1:p.Ser810=
NM_172108.4:c.2335T=	NP_742106.1:p.Ser779=
XM_011528810.2:c.2482T=	XP_011527112.1:p.Ser828=
XM_011528811.2:c.2452T=	XP_011527113.1:p.Ser818=
XM_017027841.2:c.2479T=	XP_016883330.1:p.Ser827=
XM_017027842.2:c.2416T=	XP_016883331.1:p.Ser806=
XM_017027843.1:c.2413T=	XP_016883332.1:p.Ser805=
XM_017027844.2:c.2371T=	XP_016883333.1:p.Ser791=
XM_017027845.1:c.1444T=	XP_016883334.1:p.Ser482=
NM_004518.6:c.2344T=	NP_004509.2:p.Ser782=
NM_172106.3:c.2374T=	NP_742104.1:p.Ser792=
NM_172107.4:c.2428T= MANE Select	NP_742105.1:p.Ser810=
NM_172108.5:c.2335T=	NP_742106.1:p.Ser779=
NM_001382235.1:c.2482T=	NP_001369164.1:p.Ser828=