Canonical Allele Identifier: CA409637043
Gene: KCNQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63406817C>G , CM000682.2:g.63406817C>G GRCh38
NC_000020.10:g.62038170C>G , CM000682.1:g.62038170C>G GRCh37
NC_000020.9:g.61508614C>G NCBI36
NG_009004.1:g.70824G>C
NG_009004.2:g.70824G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2500G>C ENSP00000516702.1:p.Ala834Pro
ENST00000359125.7:c.2446G>C MANE Select ENSP00000352035.2:p.Ala816Pro
ENST00000637193.1:c.1843G>C ENSP00000490734.1:p.Ala615Pro
ENST00000344462.8:c.2353G>C ENSP00000339611.4:p.Ala785Pro
ENST00000357249.6:c.2014G>C ENSP00000349789.3:p.Ala672Pro
ENST00000359125.6:c.2446G>C ENSP00000352035.2:p.Ala816Pro
ENST00000360480.7:c.2362G>C ENSP00000353668.3:p.Ala788Pro
ENST00000370224.5:c.2241+229G>C ENSP00000359244.2:n.2241+229G>C
ENST00000625514.2:c.2205+229G>C ENSP00000486040.1:n.2205+229G>C
ENST00000626839.2:c.2392G>C ENSP00000486706.1:p.Ala798Pro
ENST00000629241.2:c.2133+229G>C ENSP00000487142.1:n.2133+229G>C
ENST00000629676.2:c.1680-5974G>C ENSP00000486194.1:n.1680-5974G>C
NM_004518.4:c.2362G>C NP_004509.2:p.Ala788Pro
NM_172106.1:c.2392G>C NP_742104.1:p.Ala798Pro
NM_172107.2:c.2446G>C NP_742105.1:p.Ala816Pro
NM_172108.3:c.2353G>C NP_742106.1:p.Ala785Pro
XM_006723787.1:c.2488G>C XP_006723850.1:p.Ala830Pro
XM_011528807.1:c.2554G>C XP_011527109.1:p.Ala852Pro
XM_011528808.1:c.2551G>C XP_011527110.1:p.Ala851Pro
XM_011528809.1:c.2524G>C XP_011527111.1:p.Ala842Pro
XM_011528810.1:c.2500G>C XP_011527112.1:p.Ala834Pro
XM_011528811.1:c.2470G>C XP_011527113.1:p.Ala824Pro
XM_011528812.1:c.2443G>C XP_011527114.1:p.Ala815Pro
XM_011528813.1:c.2428G>C XP_011527115.1:p.Ala810Pro
XM_011528814.1:c.2035G>C XP_011527116.1:p.Ala679Pro
NM_004518.5:c.2362G>C NP_004509.2:p.Ala788Pro
NM_172106.2:c.2392G>C NP_742104.1:p.Ala798Pro
NM_172107.3:c.2446G>C NP_742105.1:p.Ala816Pro
NM_172108.4:c.2353G>C NP_742106.1:p.Ala785Pro
XM_011528810.2:c.2500G>C XP_011527112.1:p.Ala834Pro
XM_011528811.2:c.2470G>C XP_011527113.1:p.Ala824Pro
XM_017027841.2:c.2497G>C XP_016883330.1:p.Ala833Pro
XM_017027842.2:c.2434G>C XP_016883331.1:p.Ala812Pro
XM_017027843.1:c.2431G>C XP_016883332.1:p.Ala811Pro
XM_017027844.2:c.2389G>C XP_016883333.1:p.Ala797Pro
XM_017027845.1:c.1462G>C XP_016883334.1:p.Ala488Pro
NM_004518.6:c.2362G>C NP_004509.2:p.Ala788Pro
NM_172106.3:c.2392G>C NP_742104.1:p.Ala798Pro
NM_172107.4:c.2446G>C MANE Select NP_742105.1:p.Ala816Pro
NM_172108.5:c.2353G>C NP_742106.1:p.Ala785Pro
NM_001382235.1:c.2500G>C NP_001369164.1:p.Ala834Pro