Canonical Allele Identifier: CA2374774437
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407137G= , CM000682.2:g.63407137G= GRCh38
NC_000020.10:g.62038490G= , CM000682.1:g.62038490G= GRCh37
NC_000020.9:g.61508934G= NCBI36
NG_009004.1:g.70504C=
NG_009004.2:g.70504C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2180C= ENSP00000516702.1:p.Pro727=
ENST00000359125.7:c.2126C= MANE Select ENSP00000352035.2:p.Pro709=
ENST00000637193.1:c.1523C= ENSP00000490734.1:p.Pro508=
ENST00000344462.8:c.2033C= ENSP00000339611.4:p.Pro678=
ENST00000357249.6:c.1694C= ENSP00000349789.3:p.Pro565=
ENST00000359125.6:c.2126C= ENSP00000352035.2:p.Pro709=
ENST00000360480.7:c.2042C= ENSP00000353668.3:p.Pro681=
ENST00000370224.5:c.2150C= ENSP00000359244.2:p.Pro717=
ENST00000625514.2:c.2114C= ENSP00000486040.1:p.Pro705=
ENST00000626839.2:c.2072C= ENSP00000486706.1:p.Pro691=
ENST00000629241.2:c.2042C= ENSP00000487142.1:p.Pro681=
ENST00000629676.2:c.1680-6294C= ENSP00000486194.1:n.1680-6294C=
NM_004518.4:c.2042C= NP_004509.2:p.Pro681=
NM_172106.1:c.2072C= NP_742104.1:p.Pro691=
NM_172107.2:c.2126C= NP_742105.1:p.Pro709=
NM_172108.3:c.2033C= NP_742106.1:p.Pro678=
XM_006723787.1:c.2168C= XP_006723850.1:p.Pro723=
XM_011528807.1:c.2234C= XP_011527109.1:p.Pro745=
XM_011528808.1:c.2231C= XP_011527110.1:p.Pro744=
XM_011528809.1:c.2204C= XP_011527111.1:p.Pro735=
XM_011528810.1:c.2180C= XP_011527112.1:p.Pro727=
XM_011528811.1:c.2150C= XP_011527113.1:p.Pro717=
XM_011528812.1:c.2123C= XP_011527114.1:p.Pro708=
XM_011528813.1:c.2108C= XP_011527115.1:p.Pro703=
XM_011528814.1:c.1715C= XP_011527116.1:p.Pro572=
NM_004518.5:c.2042C= NP_004509.2:p.Pro681=
NM_172106.2:c.2072C= NP_742104.1:p.Pro691=
NM_172107.3:c.2126C= NP_742105.1:p.Pro709=
NM_172108.4:c.2033C= NP_742106.1:p.Pro678=
XM_011528810.2:c.2180C= XP_011527112.1:p.Pro727=
XM_011528811.2:c.2150C= XP_011527113.1:p.Pro717=
XM_017027841.2:c.2177C= XP_016883330.1:p.Pro726=
XM_017027842.2:c.2114C= XP_016883331.1:p.Pro705=
XM_017027843.1:c.2111C= XP_016883332.1:p.Pro704=
XM_017027844.2:c.2069C= XP_016883333.1:p.Pro690=
XM_017027845.1:c.1142C= XP_016883334.1:p.Pro381=
NM_004518.6:c.2042C= NP_004509.2:p.Pro681=
NM_172106.3:c.2072C= NP_742104.1:p.Pro691=
NM_172107.4:c.2126C= MANE Select NP_742105.1:p.Pro709=
NM_172108.5:c.2033C= NP_742106.1:p.Pro678=
NM_001382235.1:c.2180C= NP_001369164.1:p.Pro727=