Canonical Allele Identifier: CA409636940
Gene: KCNQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63406793C>A , CM000682.2:g.63406793C>A GRCh38
NC_000020.10:g.62038146C>A , CM000682.1:g.62038146C>A GRCh37
NC_000020.9:g.61508590C>A NCBI36
NG_009004.1:g.70848G>T
NG_009004.2:g.70848G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2524G>T ENSP00000516702.1:p.Val842Leu
ENST00000359125.7:c.2470G>T MANE Select ENSP00000352035.2:p.Val824Leu
ENST00000637193.1:c.1867G>T ENSP00000490734.1:p.Val623Leu
ENST00000344462.8:c.2377G>T ENSP00000339611.4:p.Val793Leu
ENST00000357249.6:c.2038G>T ENSP00000349789.3:p.Val680Leu
ENST00000359125.6:c.2470G>T ENSP00000352035.2:p.Val824Leu
ENST00000360480.7:c.2386G>T ENSP00000353668.3:p.Val796Leu
ENST00000370224.5:c.2241+253G>T ENSP00000359244.2:n.2241+253G>T
ENST00000625514.2:c.2205+253G>T ENSP00000486040.1:n.2205+253G>T
ENST00000626839.2:c.2416G>T ENSP00000486706.1:p.Val806Leu
ENST00000629241.2:c.2133+253G>T ENSP00000487142.1:n.2133+253G>T
ENST00000629676.2:c.1680-5950G>T ENSP00000486194.1:n.1680-5950G>T
NM_004518.4:c.2386G>T NP_004509.2:p.Val796Leu
NM_172106.1:c.2416G>T NP_742104.1:p.Val806Leu
NM_172107.2:c.2470G>T NP_742105.1:p.Val824Leu
NM_172108.3:c.2377G>T NP_742106.1:p.Val793Leu
XM_006723787.1:c.2512G>T XP_006723850.1:p.Val838Leu
XM_011528807.1:c.2578G>T XP_011527109.1:p.Val860Leu
XM_011528808.1:c.2575G>T XP_011527110.1:p.Val859Leu
XM_011528809.1:c.2548G>T XP_011527111.1:p.Val850Leu
XM_011528810.1:c.2524G>T XP_011527112.1:p.Val842Leu
XM_011528811.1:c.2494G>T XP_011527113.1:p.Val832Leu
XM_011528812.1:c.2467G>T XP_011527114.1:p.Val823Leu
XM_011528813.1:c.2452G>T XP_011527115.1:p.Val818Leu
XM_011528814.1:c.2059G>T XP_011527116.1:p.Val687Leu
NM_004518.5:c.2386G>T NP_004509.2:p.Val796Leu
NM_172106.2:c.2416G>T NP_742104.1:p.Val806Leu
NM_172107.3:c.2470G>T NP_742105.1:p.Val824Leu
NM_172108.4:c.2377G>T NP_742106.1:p.Val793Leu
XM_011528810.2:c.2524G>T XP_011527112.1:p.Val842Leu
XM_011528811.2:c.2494G>T XP_011527113.1:p.Val832Leu
XM_017027841.2:c.2521G>T XP_016883330.1:p.Val841Leu
XM_017027842.2:c.2458G>T XP_016883331.1:p.Val820Leu
XM_017027843.1:c.2455G>T XP_016883332.1:p.Val819Leu
XM_017027844.2:c.2413G>T XP_016883333.1:p.Val805Leu
XM_017027845.1:c.1486G>T XP_016883334.1:p.Val496Leu
NM_004518.6:c.2386G>T NP_004509.2:p.Val796Leu
NM_172106.3:c.2416G>T NP_742104.1:p.Val806Leu
NM_172107.4:c.2470G>T MANE Select NP_742105.1:p.Val824Leu
NM_172108.5:c.2377G>T NP_742106.1:p.Val793Leu
NM_001382235.1:c.2524G>T NP_001369164.1:p.Val842Leu