Canonical Allele Identifier: CA409639078

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038557C>A (hg19) ; chr20:g.63407204C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407204C>A , CM000682.2:g.63407204C>A	GRCh38
NC_000020.10:g.62038557C>A , CM000682.1:g.62038557C>A	GRCh37
NC_000020.9:g.61509001C>A	NCBI36
NG_009004.1:g.70437G>T
NG_009004.2:g.70437G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2113G>T	ENSP00000516702.1:p.Val705Phe
ENST00000359125.7:c.2059G>T MANE Select	ENSP00000352035.2:p.Val687Phe
ENST00000637193.1:c.1456G>T	ENSP00000490734.1:p.Val486Phe
ENST00000344462.8:c.1966G>T	ENSP00000339611.4:p.Val656Phe
ENST00000357249.6:c.1627G>T	ENSP00000349789.3:p.Val543Phe
ENST00000359125.6:c.2059G>T	ENSP00000352035.2:p.Val687Phe
ENST00000360480.7:c.1975G>T	ENSP00000353668.3:p.Val659Phe
ENST00000370224.5:c.2083G>T	ENSP00000359244.2:p.Val695Phe
ENST00000625514.2:c.2047G>T	ENSP00000486040.1:p.Val683Phe
ENST00000626839.2:c.2005G>T	ENSP00000486706.1:p.Val669Phe
ENST00000629241.2:c.1975G>T	ENSP00000487142.1:p.Val659Phe
ENST00000629676.2:c.1679+6246G>T	ENSP00000486194.1:n.1679+6246G>T
NM_004518.4:c.1975G>T	NP_004509.2:p.Val659Phe
NM_172106.1:c.2005G>T	NP_742104.1:p.Val669Phe
NM_172107.2:c.2059G>T	NP_742105.1:p.Val687Phe
NM_172108.3:c.1966G>T	NP_742106.1:p.Val656Phe
XM_006723787.1:c.2101G>T	XP_006723850.1:p.Val701Phe
XM_011528807.1:c.2167G>T	XP_011527109.1:p.Val723Phe
XM_011528808.1:c.2164G>T	XP_011527110.1:p.Val722Phe
XM_011528809.1:c.2137G>T	XP_011527111.1:p.Val713Phe
XM_011528810.1:c.2113G>T	XP_011527112.1:p.Val705Phe
XM_011528811.1:c.2083G>T	XP_011527113.1:p.Val695Phe
XM_011528812.1:c.2056G>T	XP_011527114.1:p.Val686Phe
XM_011528813.1:c.2041G>T	XP_011527115.1:p.Val681Phe
XM_011528814.1:c.1648G>T	XP_011527116.1:p.Val550Phe
NM_004518.5:c.1975G>T	NP_004509.2:p.Val659Phe
NM_172106.2:c.2005G>T	NP_742104.1:p.Val669Phe
NM_172107.3:c.2059G>T	NP_742105.1:p.Val687Phe
NM_172108.4:c.1966G>T	NP_742106.1:p.Val656Phe
XM_011528810.2:c.2113G>T	XP_011527112.1:p.Val705Phe
XM_011528811.2:c.2083G>T	XP_011527113.1:p.Val695Phe
XM_017027841.2:c.2110G>T	XP_016883330.1:p.Val704Phe
XM_017027842.2:c.2047G>T	XP_016883331.1:p.Val683Phe
XM_017027843.1:c.2044G>T	XP_016883332.1:p.Val682Phe
XM_017027844.2:c.2002G>T	XP_016883333.1:p.Val668Phe
XM_017027845.1:c.1075G>T	XP_016883334.1:p.Val359Phe
NM_004518.6:c.1975G>T	NP_004509.2:p.Val659Phe
NM_172106.3:c.2005G>T	NP_742104.1:p.Val669Phe
NM_172107.4:c.2059G>T MANE Select	NP_742105.1:p.Val687Phe
NM_172108.5:c.1966G>T	NP_742106.1:p.Val656Phe
NM_001382235.1:c.2113G>T	NP_001369164.1:p.Val705Phe