Canonical Allele Identifier: CA409639530

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038709T>A (hg19) ; chr20:g.63407356T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407356T>A , CM000682.2:g.63407356T>A	GRCh38
NC_000020.10:g.62038709T>A , CM000682.1:g.62038709T>A	GRCh37
NC_000020.9:g.61509153T>A	NCBI36
NG_009004.1:g.70285A>T
NG_009004.2:g.70285A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1961A>T	ENSP00000516702.1:p.Lys654Met
ENST00000359125.7:c.1907A>T MANE Select	ENSP00000352035.2:p.Lys636Met
ENST00000637193.1:c.1304A>T	ENSP00000490734.1:p.Lys435Met
ENST00000637338.1:n.64A>T
ENST00000344462.8:c.1814A>T	ENSP00000339611.4:p.Lys605Met
ENST00000357249.6:c.1475A>T	ENSP00000349789.3:p.Lys492Met
ENST00000359125.6:c.1907A>T	ENSP00000352035.2:p.Lys636Met
ENST00000360480.7:c.1823A>T	ENSP00000353668.3:p.Lys608Met
ENST00000370224.5:c.1931A>T	ENSP00000359244.2:p.Lys644Met
ENST00000625514.2:c.1895A>T	ENSP00000486040.1:p.Lys632Met
ENST00000626839.2:c.1853A>T	ENSP00000486706.1:p.Lys618Met
ENST00000629241.2:c.1823A>T	ENSP00000487142.1:p.Lys608Met
ENST00000629676.2:c.1679+6094A>T	ENSP00000486194.1:n.1679+6094A>T
NM_004518.4:c.1823A>T	NP_004509.2:p.Lys608Met
NM_172106.1:c.1853A>T	NP_742104.1:p.Lys618Met
NM_172107.2:c.1907A>T	NP_742105.1:p.Lys636Met
NM_172108.3:c.1814A>T	NP_742106.1:p.Lys605Met
XM_006723787.1:c.1949A>T	XP_006723850.1:p.Lys650Met
XM_011528807.1:c.2015A>T	XP_011527109.1:p.Lys672Met
XM_011528808.1:c.2012A>T	XP_011527110.1:p.Lys671Met
XM_011528809.1:c.1985A>T	XP_011527111.1:p.Lys662Met
XM_011528810.1:c.1961A>T	XP_011527112.1:p.Lys654Met
XM_011528811.1:c.1931A>T	XP_011527113.1:p.Lys644Met
XM_011528812.1:c.1904A>T	XP_011527114.1:p.Lys635Met
XM_011528813.1:c.1889A>T	XP_011527115.1:p.Lys630Met
XM_011528814.1:c.1496A>T	XP_011527116.1:p.Lys499Met
NM_004518.5:c.1823A>T	NP_004509.2:p.Lys608Met
NM_172106.2:c.1853A>T	NP_742104.1:p.Lys618Met
NM_172107.3:c.1907A>T	NP_742105.1:p.Lys636Met
NM_172108.4:c.1814A>T	NP_742106.1:p.Lys605Met
XM_011528810.2:c.1961A>T	XP_011527112.1:p.Lys654Met
XM_011528811.2:c.1931A>T	XP_011527113.1:p.Lys644Met
XM_017027841.2:c.1958A>T	XP_016883330.1:p.Lys653Met
XM_017027842.2:c.1895A>T	XP_016883331.1:p.Lys632Met
XM_017027843.1:c.1892A>T	XP_016883332.1:p.Lys631Met
XM_017027844.2:c.1850A>T	XP_016883333.1:p.Lys617Met
XM_017027845.1:c.923A>T	XP_016883334.1:p.Lys308Met
NM_004518.6:c.1823A>T	NP_004509.2:p.Lys608Met
NM_172106.3:c.1853A>T	NP_742104.1:p.Lys618Met
NM_172107.4:c.1907A>T MANE Select	NP_742105.1:p.Lys636Met
NM_172108.5:c.1814A>T	NP_742106.1:p.Lys605Met
NM_001382235.1:c.1961A>T	NP_001369164.1:p.Lys654Met