Canonical Allele Identifier: CA409637992

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038327C>A (hg19) ; chr20:g.63406974C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406974C>A , CM000682.2:g.63406974C>A	GRCh38
NC_000020.10:g.62038327C>A , CM000682.1:g.62038327C>A	GRCh37
NC_000020.9:g.61508771C>A	NCBI36
NG_009004.1:g.70667G>T
NG_009004.2:g.70667G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2343G>T	ENSP00000516702.1:p.Met781Ile
ENST00000359125.7:c.2289G>T MANE Select	ENSP00000352035.2:p.Met763Ile
ENST00000637193.1:c.1686G>T	ENSP00000490734.1:p.Met562Ile
ENST00000344462.8:c.2196G>T	ENSP00000339611.4:p.Met732Ile
ENST00000357249.6:c.1857G>T	ENSP00000349789.3:p.Met619Ile
ENST00000359125.6:c.2289G>T	ENSP00000352035.2:p.Met763Ile
ENST00000360480.7:c.2205G>T	ENSP00000353668.3:p.Met735Ile
ENST00000370224.5:c.2241+72G>T	ENSP00000359244.2:n.2241+72G>T
ENST00000625514.2:c.2205+72G>T	ENSP00000486040.1:n.2205+72G>T
ENST00000626839.2:c.2235G>T	ENSP00000486706.1:p.Met745Ile
ENST00000629241.2:c.2133+72G>T	ENSP00000487142.1:n.2133+72G>T
ENST00000629676.2:c.1680-6131G>T	ENSP00000486194.1:n.1680-6131G>T
NM_004518.4:c.2205G>T	NP_004509.2:p.Met735Ile
NM_172106.1:c.2235G>T	NP_742104.1:p.Met745Ile
NM_172107.2:c.2289G>T	NP_742105.1:p.Met763Ile
NM_172108.3:c.2196G>T	NP_742106.1:p.Met732Ile
XM_006723787.1:c.2331G>T	XP_006723850.1:p.Met777Ile
XM_011528807.1:c.2397G>T	XP_011527109.1:p.Met799Ile
XM_011528808.1:c.2394G>T	XP_011527110.1:p.Met798Ile
XM_011528809.1:c.2367G>T	XP_011527111.1:p.Met789Ile
XM_011528810.1:c.2343G>T	XP_011527112.1:p.Met781Ile
XM_011528811.1:c.2313G>T	XP_011527113.1:p.Met771Ile
XM_011528812.1:c.2286G>T	XP_011527114.1:p.Met762Ile
XM_011528813.1:c.2271G>T	XP_011527115.1:p.Met757Ile
XM_011528814.1:c.1878G>T	XP_011527116.1:p.Met626Ile
NM_004518.5:c.2205G>T	NP_004509.2:p.Met735Ile
NM_172106.2:c.2235G>T	NP_742104.1:p.Met745Ile
NM_172107.3:c.2289G>T	NP_742105.1:p.Met763Ile
NM_172108.4:c.2196G>T	NP_742106.1:p.Met732Ile
XM_011528810.2:c.2343G>T	XP_011527112.1:p.Met781Ile
XM_011528811.2:c.2313G>T	XP_011527113.1:p.Met771Ile
XM_017027841.2:c.2340G>T	XP_016883330.1:p.Met780Ile
XM_017027842.2:c.2277G>T	XP_016883331.1:p.Met759Ile
XM_017027843.1:c.2274G>T	XP_016883332.1:p.Met758Ile
XM_017027844.2:c.2232G>T	XP_016883333.1:p.Met744Ile
XM_017027845.1:c.1305G>T	XP_016883334.1:p.Met435Ile
NM_004518.6:c.2205G>T	NP_004509.2:p.Met735Ile
NM_172106.3:c.2235G>T	NP_742104.1:p.Met745Ile
NM_172107.4:c.2289G>T MANE Select	NP_742105.1:p.Met763Ile
NM_172108.5:c.2196G>T	NP_742106.1:p.Met732Ile
NM_001382235.1:c.2343G>T	NP_001369164.1:p.Met781Ile