Canonical Allele Identifier: CA409639175

Gene: KCNQ2

Linked Data

• gnomAD v4: 20-63407246-G-T
• MyVariant Identifiers: chr20:g.62038599G>T (hg19) ; chr20:g.63407246G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407246G>T , CM000682.2:g.63407246G>T	GRCh38
NC_000020.10:g.62038599G>T , CM000682.1:g.62038599G>T	GRCh37
NC_000020.9:g.61509043G>T	NCBI36
NG_009004.1:g.70395C>A
NG_009004.2:g.70395C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2071C>A	ENSP00000516702.1:p.Pro691Thr
ENST00000359125.7:c.2017C>A MANE Select	ENSP00000352035.2:p.Pro673Thr
ENST00000637193.1:c.1414C>A	ENSP00000490734.1:p.Pro472Thr
ENST00000344462.8:c.1924C>A	ENSP00000339611.4:p.Pro642Thr
ENST00000357249.6:c.1585C>A	ENSP00000349789.3:p.Pro529Thr
ENST00000359125.6:c.2017C>A	ENSP00000352035.2:p.Pro673Thr
ENST00000360480.7:c.1933C>A	ENSP00000353668.3:p.Pro645Thr
ENST00000370224.5:c.2041C>A	ENSP00000359244.2:p.Pro681Thr
ENST00000625514.2:c.2005C>A	ENSP00000486040.1:p.Pro669Thr
ENST00000626839.2:c.1963C>A	ENSP00000486706.1:p.Pro655Thr
ENST00000629241.2:c.1933C>A	ENSP00000487142.1:p.Pro645Thr
ENST00000629676.2:c.1679+6204C>A	ENSP00000486194.1:n.1679+6204C>A
NM_004518.4:c.1933C>A	NP_004509.2:p.Pro645Thr
NM_172106.1:c.1963C>A	NP_742104.1:p.Pro655Thr
NM_172107.2:c.2017C>A	NP_742105.1:p.Pro673Thr
NM_172108.3:c.1924C>A	NP_742106.1:p.Pro642Thr
XM_006723787.1:c.2059C>A	XP_006723850.1:p.Pro687Thr
XM_011528807.1:c.2125C>A	XP_011527109.1:p.Pro709Thr
XM_011528808.1:c.2122C>A	XP_011527110.1:p.Pro708Thr
XM_011528809.1:c.2095C>A	XP_011527111.1:p.Pro699Thr
XM_011528810.1:c.2071C>A	XP_011527112.1:p.Pro691Thr
XM_011528811.1:c.2041C>A	XP_011527113.1:p.Pro681Thr
XM_011528812.1:c.2014C>A	XP_011527114.1:p.Pro672Thr
XM_011528813.1:c.1999C>A	XP_011527115.1:p.Pro667Thr
XM_011528814.1:c.1606C>A	XP_011527116.1:p.Pro536Thr
NM_004518.5:c.1933C>A	NP_004509.2:p.Pro645Thr
NM_172106.2:c.1963C>A	NP_742104.1:p.Pro655Thr
NM_172107.3:c.2017C>A	NP_742105.1:p.Pro673Thr
NM_172108.4:c.1924C>A	NP_742106.1:p.Pro642Thr
XM_011528810.2:c.2071C>A	XP_011527112.1:p.Pro691Thr
XM_011528811.2:c.2041C>A	XP_011527113.1:p.Pro681Thr
XM_017027841.2:c.2068C>A	XP_016883330.1:p.Pro690Thr
XM_017027842.2:c.2005C>A	XP_016883331.1:p.Pro669Thr
XM_017027843.1:c.2002C>A	XP_016883332.1:p.Pro668Thr
XM_017027844.2:c.1960C>A	XP_016883333.1:p.Pro654Thr
XM_017027845.1:c.1033C>A	XP_016883334.1:p.Pro345Thr
NM_004518.6:c.1933C>A	NP_004509.2:p.Pro645Thr
NM_172106.3:c.1963C>A	NP_742104.1:p.Pro655Thr
NM_172107.4:c.2017C>A MANE Select	NP_742105.1:p.Pro673Thr
NM_172108.5:c.1924C>A	NP_742106.1:p.Pro642Thr
NM_001382235.1:c.2071C>A	NP_001369164.1:p.Pro691Thr