Canonical Allele Identifier: CA409639379

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038674T>C (hg19) ; chr20:g.63407321T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407321T>C , CM000682.2:g.63407321T>C	GRCh38
NC_000020.10:g.62038674T>C , CM000682.1:g.62038674T>C	GRCh37
NC_000020.9:g.61509118T>C	NCBI36
NG_009004.1:g.70320A>G
NG_009004.2:g.70320A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1996A>G	ENSP00000516702.1:p.Met666Val
ENST00000359125.7:c.1942A>G MANE Select	ENSP00000352035.2:p.Met648Val
ENST00000637193.1:c.1339A>G	ENSP00000490734.1:p.Met447Val
ENST00000637338.1:n.99A>G
ENST00000344462.8:c.1849A>G	ENSP00000339611.4:p.Met617Val
ENST00000357249.6:c.1510A>G	ENSP00000349789.3:p.Met504Val
ENST00000359125.6:c.1942A>G	ENSP00000352035.2:p.Met648Val
ENST00000360480.7:c.1858A>G	ENSP00000353668.3:p.Met620Val
ENST00000370224.5:c.1966A>G	ENSP00000359244.2:p.Met656Val
ENST00000625514.2:c.1930A>G	ENSP00000486040.1:p.Met644Val
ENST00000626839.2:c.1888A>G	ENSP00000486706.1:p.Met630Val
ENST00000629241.2:c.1858A>G	ENSP00000487142.1:p.Met620Val
ENST00000629676.2:c.1679+6129A>G	ENSP00000486194.1:n.1679+6129A>G
NM_004518.4:c.1858A>G	NP_004509.2:p.Met620Val
NM_172106.1:c.1888A>G	NP_742104.1:p.Met630Val
NM_172107.2:c.1942A>G	NP_742105.1:p.Met648Val
NM_172108.3:c.1849A>G	NP_742106.1:p.Met617Val
XM_006723787.1:c.1984A>G	XP_006723850.1:p.Met662Val
XM_011528807.1:c.2050A>G	XP_011527109.1:p.Met684Val
XM_011528808.1:c.2047A>G	XP_011527110.1:p.Met683Val
XM_011528809.1:c.2020A>G	XP_011527111.1:p.Met674Val
XM_011528810.1:c.1996A>G	XP_011527112.1:p.Met666Val
XM_011528811.1:c.1966A>G	XP_011527113.1:p.Met656Val
XM_011528812.1:c.1939A>G	XP_011527114.1:p.Met647Val
XM_011528813.1:c.1924A>G	XP_011527115.1:p.Met642Val
XM_011528814.1:c.1531A>G	XP_011527116.1:p.Met511Val
NM_004518.5:c.1858A>G	NP_004509.2:p.Met620Val
NM_172106.2:c.1888A>G	NP_742104.1:p.Met630Val
NM_172107.3:c.1942A>G	NP_742105.1:p.Met648Val
NM_172108.4:c.1849A>G	NP_742106.1:p.Met617Val
XM_011528810.2:c.1996A>G	XP_011527112.1:p.Met666Val
XM_011528811.2:c.1966A>G	XP_011527113.1:p.Met656Val
XM_017027841.2:c.1993A>G	XP_016883330.1:p.Met665Val
XM_017027842.2:c.1930A>G	XP_016883331.1:p.Met644Val
XM_017027843.1:c.1927A>G	XP_016883332.1:p.Met643Val
XM_017027844.2:c.1885A>G	XP_016883333.1:p.Met629Val
XM_017027845.1:c.958A>G	XP_016883334.1:p.Met320Val
NM_004518.6:c.1858A>G	NP_004509.2:p.Met620Val
NM_172106.3:c.1888A>G	NP_742104.1:p.Met630Val
NM_172107.4:c.1942A>G MANE Select	NP_742105.1:p.Met648Val
NM_172108.5:c.1849A>G	NP_742106.1:p.Met617Val
NM_001382235.1:c.1996A>G	NP_001369164.1:p.Met666Val