Canonical Allele Identifier: CA511339313

Gene: KCNQ2

Linked Data

• gnomAD v4: 20-63406794-G-C
• MyVariant Identifiers: chr20:g.62038147G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406794G>C , CM000682.2:g.63406794G>C	GRCh38
NC_000020.10:g.62038147G>C , CM000682.1:g.62038147G>C	GRCh37
NC_000020.9:g.61508591G>C	NCBI36
NG_009004.1:g.70847C>G
NG_009004.2:g.70847C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2523C>G	ENSP00000516702.1:p.Ala841=
ENST00000359125.7:c.2469C>G MANE Select	ENSP00000352035.2:p.Ala823=
ENST00000637193.1:c.1866C>G	ENSP00000490734.1:p.Ala622=
ENST00000344462.8:c.2376C>G	ENSP00000339611.4:p.Ala792=
ENST00000357249.6:c.2037C>G	ENSP00000349789.3:p.Ala679=
ENST00000359125.6:c.2469C>G	ENSP00000352035.2:p.Ala823=
ENST00000360480.7:c.2385C>G	ENSP00000353668.3:p.Ala795=
ENST00000370224.5:c.2241+252C>G	ENSP00000359244.2:n.2241+252C>G
ENST00000625514.2:c.2205+252C>G	ENSP00000486040.1:n.2205+252C>G
ENST00000626839.2:c.2415C>G	ENSP00000486706.1:p.Ala805=
ENST00000629241.2:c.2133+252C>G	ENSP00000487142.1:n.2133+252C>G
ENST00000629676.2:c.1680-5951C>G	ENSP00000486194.1:n.1680-5951C>G
NM_004518.4:c.2385C>G	NP_004509.2:p.Ala795=
NM_172106.1:c.2415C>G	NP_742104.1:p.Ala805=
NM_172107.2:c.2469C>G	NP_742105.1:p.Ala823=
NM_172108.3:c.2376C>G	NP_742106.1:p.Ala792=
XM_006723787.1:c.2511C>G	XP_006723850.1:p.Ala837=
XM_011528807.1:c.2577C>G	XP_011527109.1:p.Ala859=
XM_011528808.1:c.2574C>G	XP_011527110.1:p.Ala858=
XM_011528809.1:c.2547C>G	XP_011527111.1:p.Ala849=
XM_011528810.1:c.2523C>G	XP_011527112.1:p.Ala841=
XM_011528811.1:c.2493C>G	XP_011527113.1:p.Ala831=
XM_011528812.1:c.2466C>G	XP_011527114.1:p.Ala822=
XM_011528813.1:c.2451C>G	XP_011527115.1:p.Ala817=
XM_011528814.1:c.2058C>G	XP_011527116.1:p.Ala686=
NM_004518.5:c.2385C>G	NP_004509.2:p.Ala795=
NM_172106.2:c.2415C>G	NP_742104.1:p.Ala805=
NM_172107.3:c.2469C>G	NP_742105.1:p.Ala823=
NM_172108.4:c.2376C>G	NP_742106.1:p.Ala792=
XM_011528810.2:c.2523C>G	XP_011527112.1:p.Ala841=
XM_011528811.2:c.2493C>G	XP_011527113.1:p.Ala831=
XM_017027841.2:c.2520C>G	XP_016883330.1:p.Ala840=
XM_017027842.2:c.2457C>G	XP_016883331.1:p.Ala819=
XM_017027843.1:c.2454C>G	XP_016883332.1:p.Ala818=
XM_017027844.2:c.2412C>G	XP_016883333.1:p.Ala804=
XM_017027845.1:c.1485C>G	XP_016883334.1:p.Ala495=
NM_004518.6:c.2385C>G	NP_004509.2:p.Ala795=
NM_172106.3:c.2415C>G	NP_742104.1:p.Ala805=
NM_172107.4:c.2469C>G MANE Select	NP_742105.1:p.Ala823=
NM_172108.5:c.2376C>G	NP_742106.1:p.Ala792=
NM_001382235.1:c.2523C>G	NP_001369164.1:p.Ala841=