Canonical Allele Identifier: CA409636450

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038031A>T (hg19) ; chr20:g.63406678A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406678A>T , CM000682.2:g.63406678A>T	GRCh38
NC_000020.10:g.62038031A>T , CM000682.1:g.62038031A>T	GRCh37
NC_000020.9:g.61508475A>T	NCBI36
NG_009004.1:g.70963T>A
NG_009004.2:g.70963T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2639T>A	ENSP00000516702.1:p.Phe880Tyr
ENST00000359125.7:c.2585T>A MANE Select	ENSP00000352035.2:p.Phe862Tyr
ENST00000637193.1:c.1982T>A	ENSP00000490734.1:p.Phe661Tyr
ENST00000344462.8:c.2492T>A	ENSP00000339611.4:p.Phe831Tyr
ENST00000357249.6:c.2153T>A	ENSP00000349789.3:p.Phe718Tyr
ENST00000359125.6:c.2585T>A	ENSP00000352035.2:p.Phe862Tyr
ENST00000360480.7:c.2501T>A	ENSP00000353668.3:p.Phe834Tyr
ENST00000370224.5:c.2241+368T>A	ENSP00000359244.2:n.2241+368T>A
ENST00000625514.2:c.2205+368T>A	ENSP00000486040.1:n.2205+368T>A
ENST00000626839.2:c.2531T>A	ENSP00000486706.1:p.Phe844Tyr
ENST00000629241.2:c.2133+368T>A	ENSP00000487142.1:n.2133+368T>A
ENST00000629676.2:c.1680-5835T>A	ENSP00000486194.1:n.1680-5835T>A
NM_004518.4:c.2501T>A	NP_004509.2:p.Phe834Tyr
NM_172106.1:c.2531T>A	NP_742104.1:p.Phe844Tyr
NM_172107.2:c.2585T>A	NP_742105.1:p.Phe862Tyr
NM_172108.3:c.2492T>A	NP_742106.1:p.Phe831Tyr
XM_006723787.1:c.2627T>A	XP_006723850.1:p.Phe876Tyr
XM_011528807.1:c.2693T>A	XP_011527109.1:p.Phe898Tyr
XM_011528808.1:c.2690T>A	XP_011527110.1:p.Phe897Tyr
XM_011528809.1:c.2663T>A	XP_011527111.1:p.Phe888Tyr
XM_011528810.1:c.2639T>A	XP_011527112.1:p.Phe880Tyr
XM_011528811.1:c.2609T>A	XP_011527113.1:p.Phe870Tyr
XM_011528812.1:c.2582T>A	XP_011527114.1:p.Phe861Tyr
XM_011528813.1:c.2567T>A	XP_011527115.1:p.Phe856Tyr
XM_011528814.1:c.2174T>A	XP_011527116.1:p.Phe725Tyr
NM_004518.5:c.2501T>A	NP_004509.2:p.Phe834Tyr
NM_172106.2:c.2531T>A	NP_742104.1:p.Phe844Tyr
NM_172107.3:c.2585T>A	NP_742105.1:p.Phe862Tyr
NM_172108.4:c.2492T>A	NP_742106.1:p.Phe831Tyr
XM_011528810.2:c.2639T>A	XP_011527112.1:p.Phe880Tyr
XM_011528811.2:c.2609T>A	XP_011527113.1:p.Phe870Tyr
XM_017027841.2:c.2636T>A	XP_016883330.1:p.Phe879Tyr
XM_017027842.2:c.2573T>A	XP_016883331.1:p.Phe858Tyr
XM_017027843.1:c.2570T>A	XP_016883332.1:p.Phe857Tyr
XM_017027844.2:c.2528T>A	XP_016883333.1:p.Phe843Tyr
XM_017027845.1:c.1601T>A	XP_016883334.1:p.Phe534Tyr
NM_004518.6:c.2501T>A	NP_004509.2:p.Phe834Tyr
NM_172106.3:c.2531T>A	NP_742104.1:p.Phe844Tyr
NM_172107.4:c.2585T>A MANE Select	NP_742105.1:p.Phe862Tyr
NM_172108.5:c.2492T>A	NP_742106.1:p.Phe831Tyr
NM_001382235.1:c.2639T>A	NP_001369164.1:p.Phe880Tyr