Canonical Allele Identifier: CA2577453420

Gene: KCNQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63414028_63414041del , CM000682.2:g.63414028_63414041del	GRCh38
NC_000020.10:g.62045381_62045394del , CM000682.1:g.62045381_62045394del	GRCh37
NC_000020.9:g.61515825_61515838del	NCBI36
NG_009004.1:g.63600_63613del
NG_009004.2:g.63600_63613del

Transcript Alleles

HGVS	Amino-acid change
ENST00000706989.1:c.1577+47_1577+60del	ENSP00000516702.1:n.1577+47_1577+60del
ENST00000359125.7:c.1631+47_1631+60del MANE Select	ENSP00000352035.2:n.1631+47_1631+60del
ENST00000637193.1:c.1028+47_1028+60del	ENSP00000490734.1:n.1028+47_1028+60del
ENST00000344462.8:c.1538+47_1538+60del	ENSP00000339611.4:n.1538+47_1538+60del
ENST00000357249.6:c.1199+47_1199+60del	ENSP00000349789.3:n.1199+47_1199+60del
ENST00000359125.6:c.1631+47_1631+60del	ENSP00000352035.2:n.1631+47_1631+60del
ENST00000360480.7:c.1547+47_1547+60del	ENSP00000353668.3:n.1547+47_1547+60del
ENST00000370224.5:c.1547+47_1547+60del	ENSP00000359244.2:n.1547+47_1547+60del
ENST00000625514.2:c.1511+47_1511+60del	ENSP00000486040.1:n.1511+47_1511+60del
ENST00000626839.2:c.1577+47_1577+60del	ENSP00000486706.1:n.1577+47_1577+60del
ENST00000629241.2:c.1547+47_1547+60del	ENSP00000487142.1:n.1547+47_1547+60del
ENST00000629318.1:c.239+47_239+60del	ENSP00000487384.1:n.239+47_239+60del
ENST00000629676.2:c.1547+47_1547+60del	ENSP00000486194.1:n.1547+47_1547+60del
NM_004518.4:c.1547+47_1547+60del	NP_004509.2:n.1547+47_1547+60del
NM_172106.1:c.1577+47_1577+60del	NP_742104.1:n.1577+47_1577+60del
NM_172107.2:c.1631+47_1631+60del	NP_742105.1:n.1631+47_1631+60del
NM_172108.3:c.1538+47_1538+60del	NP_742106.1:n.1538+47_1538+60del
XM_006723787.1:c.1631+47_1631+60del	XP_006723850.1:n.1631+47_1631+60del
XM_011528807.1:c.1631+47_1631+60del	XP_011527109.1:n.1631+47_1631+60del
XM_011528808.1:c.1628+47_1628+60del	XP_011527110.1:n.1628+47_1628+60del
XM_011528809.1:c.1601+47_1601+60del	XP_011527111.1:n.1601+47_1601+60del
XM_011528810.1:c.1577+47_1577+60del	XP_011527112.1:n.1577+47_1577+60del
XM_011528811.1:c.1547+47_1547+60del	XP_011527113.1:n.1547+47_1547+60del
XM_011528812.1:c.1628+47_1628+60del	XP_011527114.1:n.1628+47_1628+60del
XM_011528813.1:c.1505+47_1505+60del	XP_011527115.1:n.1505+47_1505+60del
XM_011528814.1:c.1112+47_1112+60del	XP_011527116.1:n.1112+47_1112+60del
XM_011528815.1:c.1631+47_1631+60del	XP_011527117.1:n.1631+47_1631+60del
NM_004518.5:c.1547+47_1547+60del	NP_004509.2:n.1547+47_1547+60del
NM_172106.2:c.1577+47_1577+60del	NP_742104.1:n.1577+47_1577+60del
NM_172107.3:c.1631+47_1631+60del	NP_742105.1:n.1631+47_1631+60del
NM_172108.4:c.1538+47_1538+60del	NP_742106.1:n.1538+47_1538+60del
XM_011528810.2:c.1577+47_1577+60del	XP_011527112.1:n.1577+47_1577+60del
XM_011528811.2:c.1547+47_1547+60del	XP_011527113.1:n.1547+47_1547+60del
XM_017027841.2:c.1574+47_1574+60del	XP_016883330.1:n.1574+47_1574+60del
XM_017027842.2:c.1577+47_1577+60del	XP_016883331.1:n.1577+47_1577+60del
XM_017027843.1:c.1508+47_1508+60del	XP_016883332.1:n.1508+47_1508+60del
XM_017027844.2:c.1574+47_1574+60del	XP_016883333.1:n.1574+47_1574+60del
XM_017027845.1:c.539+47_539+60del	XP_016883334.1:n.539+47_539+60del
NM_004518.6:c.1547+47_1547+60del	NP_004509.2:n.1547+47_1547+60del
NM_172106.3:c.1577+47_1577+60del	NP_742104.1:n.1577+47_1577+60del
NM_172107.4:c.1631+47_1631+60del MANE Select	NP_742105.1:n.1631+47_1631+60del
NM_172108.5:c.1538+47_1538+60del	NP_742106.1:n.1538+47_1538+60del
NM_001382235.1:c.1577+47_1577+60del	NP_001369164.1:n.1577+47_1577+60del