Canonical Allele Identifier: CA409637618

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038269C>G (hg19) ; chr20:g.63406916C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406916C>G , CM000682.2:g.63406916C>G	GRCh38
NC_000020.10:g.62038269C>G , CM000682.1:g.62038269C>G	GRCh37
NC_000020.9:g.61508713C>G	NCBI36
NG_009004.1:g.70725G>C
NG_009004.2:g.70725G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2401G>C	ENSP00000516702.1:p.Asp801His
ENST00000359125.7:c.2347G>C MANE Select	ENSP00000352035.2:p.Asp783His
ENST00000637193.1:c.1744G>C	ENSP00000490734.1:p.Asp582His
ENST00000344462.8:c.2254G>C	ENSP00000339611.4:p.Asp752His
ENST00000357249.6:c.1915G>C	ENSP00000349789.3:p.Asp639His
ENST00000359125.6:c.2347G>C	ENSP00000352035.2:p.Asp783His
ENST00000360480.7:c.2263G>C	ENSP00000353668.3:p.Asp755His
ENST00000370224.5:c.2241+130G>C	ENSP00000359244.2:n.2241+130G>C
ENST00000625514.2:c.2205+130G>C	ENSP00000486040.1:n.2205+130G>C
ENST00000626839.2:c.2293G>C	ENSP00000486706.1:p.Asp765His
ENST00000629241.2:c.2133+130G>C	ENSP00000487142.1:n.2133+130G>C
ENST00000629676.2:c.1680-6073G>C	ENSP00000486194.1:n.1680-6073G>C
NM_004518.4:c.2263G>C	NP_004509.2:p.Asp755His
NM_172106.1:c.2293G>C	NP_742104.1:p.Asp765His
NM_172107.2:c.2347G>C	NP_742105.1:p.Asp783His
NM_172108.3:c.2254G>C	NP_742106.1:p.Asp752His
XM_006723787.1:c.2389G>C	XP_006723850.1:p.Asp797His
XM_011528807.1:c.2455G>C	XP_011527109.1:p.Asp819His
XM_011528808.1:c.2452G>C	XP_011527110.1:p.Asp818His
XM_011528809.1:c.2425G>C	XP_011527111.1:p.Asp809His
XM_011528810.1:c.2401G>C	XP_011527112.1:p.Asp801His
XM_011528811.1:c.2371G>C	XP_011527113.1:p.Asp791His
XM_011528812.1:c.2344G>C	XP_011527114.1:p.Asp782His
XM_011528813.1:c.2329G>C	XP_011527115.1:p.Asp777His
XM_011528814.1:c.1936G>C	XP_011527116.1:p.Asp646His
NM_004518.5:c.2263G>C	NP_004509.2:p.Asp755His
NM_172106.2:c.2293G>C	NP_742104.1:p.Asp765His
NM_172107.3:c.2347G>C	NP_742105.1:p.Asp783His
NM_172108.4:c.2254G>C	NP_742106.1:p.Asp752His
XM_011528810.2:c.2401G>C	XP_011527112.1:p.Asp801His
XM_011528811.2:c.2371G>C	XP_011527113.1:p.Asp791His
XM_017027841.2:c.2398G>C	XP_016883330.1:p.Asp800His
XM_017027842.2:c.2335G>C	XP_016883331.1:p.Asp779His
XM_017027843.1:c.2332G>C	XP_016883332.1:p.Asp778His
XM_017027844.2:c.2290G>C	XP_016883333.1:p.Asp764His
XM_017027845.1:c.1363G>C	XP_016883334.1:p.Asp455His
NM_004518.6:c.2263G>C	NP_004509.2:p.Asp755His
NM_172106.3:c.2293G>C	NP_742104.1:p.Asp765His
NM_172107.4:c.2347G>C MANE Select	NP_742105.1:p.Asp783His
NM_172108.5:c.2254G>C	NP_742106.1:p.Asp752His
NM_001382235.1:c.2401G>C	NP_001369164.1:p.Asp801His