Canonical Allele Identifier: CA409639591

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038719T>A (hg19) ; chr20:g.63407366T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407366T>A , CM000682.2:g.63407366T>A	GRCh38
NC_000020.10:g.62038719T>A , CM000682.1:g.62038719T>A	GRCh37
NC_000020.9:g.61509163T>A	NCBI36
NG_009004.1:g.70275A>T
NG_009004.2:g.70275A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1951A>T	ENSP00000516702.1:p.Met651Leu
ENST00000359125.7:c.1897A>T MANE Select	ENSP00000352035.2:p.Met633Leu
ENST00000637193.1:c.1294A>T	ENSP00000490734.1:p.Met432Leu
ENST00000637338.1:n.54A>T
ENST00000344462.8:c.1804A>T	ENSP00000339611.4:p.Met602Leu
ENST00000357249.6:c.1465A>T	ENSP00000349789.3:p.Met489Leu
ENST00000359125.6:c.1897A>T	ENSP00000352035.2:p.Met633Leu
ENST00000360480.7:c.1813A>T	ENSP00000353668.3:p.Met605Leu
ENST00000370224.5:c.1921A>T	ENSP00000359244.2:p.Met641Leu
ENST00000625514.2:c.1885A>T	ENSP00000486040.1:p.Met629Leu
ENST00000626839.2:c.1843A>T	ENSP00000486706.1:p.Met615Leu
ENST00000629241.2:c.1813A>T	ENSP00000487142.1:p.Met605Leu
ENST00000629676.2:c.1679+6084A>T	ENSP00000486194.1:n.1679+6084A>T
NM_004518.4:c.1813A>T	NP_004509.2:p.Met605Leu
NM_172106.1:c.1843A>T	NP_742104.1:p.Met615Leu
NM_172107.2:c.1897A>T	NP_742105.1:p.Met633Leu
NM_172108.3:c.1804A>T	NP_742106.1:p.Met602Leu
XM_006723787.1:c.1939A>T	XP_006723850.1:p.Met647Leu
XM_011528807.1:c.2005A>T	XP_011527109.1:p.Met669Leu
XM_011528808.1:c.2002A>T	XP_011527110.1:p.Met668Leu
XM_011528809.1:c.1975A>T	XP_011527111.1:p.Met659Leu
XM_011528810.1:c.1951A>T	XP_011527112.1:p.Met651Leu
XM_011528811.1:c.1921A>T	XP_011527113.1:p.Met641Leu
XM_011528812.1:c.1894A>T	XP_011527114.1:p.Met632Leu
XM_011528813.1:c.1879A>T	XP_011527115.1:p.Met627Leu
XM_011528814.1:c.1486A>T	XP_011527116.1:p.Met496Leu
NM_004518.5:c.1813A>T	NP_004509.2:p.Met605Leu
NM_172106.2:c.1843A>T	NP_742104.1:p.Met615Leu
NM_172107.3:c.1897A>T	NP_742105.1:p.Met633Leu
NM_172108.4:c.1804A>T	NP_742106.1:p.Met602Leu
XM_011528810.2:c.1951A>T	XP_011527112.1:p.Met651Leu
XM_011528811.2:c.1921A>T	XP_011527113.1:p.Met641Leu
XM_017027841.2:c.1948A>T	XP_016883330.1:p.Met650Leu
XM_017027842.2:c.1885A>T	XP_016883331.1:p.Met629Leu
XM_017027843.1:c.1882A>T	XP_016883332.1:p.Met628Leu
XM_017027844.2:c.1840A>T	XP_016883333.1:p.Met614Leu
XM_017027845.1:c.913A>T	XP_016883334.1:p.Met305Leu
NM_004518.6:c.1813A>T	NP_004509.2:p.Met605Leu
NM_172106.3:c.1843A>T	NP_742104.1:p.Met615Leu
NM_172107.4:c.1897A>T MANE Select	NP_742105.1:p.Met633Leu
NM_172108.5:c.1804A>T	NP_742106.1:p.Met602Leu
NM_001382235.1:c.1951A>T	NP_001369164.1:p.Met651Leu