Canonical Allele Identifier: CA409639368

Gene: KCNQ2

Linked Data

• gnomAD v4: 20-63407319-C-A
• MyVariant Identifiers: chr20:g.62038672C>A (hg19) ; chr20:g.63407319C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407319C>A , CM000682.2:g.63407319C>A	GRCh38
NC_000020.10:g.62038672C>A , CM000682.1:g.62038672C>A	GRCh37
NC_000020.9:g.61509116C>A	NCBI36
NG_009004.1:g.70322G>T
NG_009004.2:g.70322G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1998G>T	ENSP00000516702.1:p.Met666Ile
ENST00000359125.7:c.1944G>T MANE Select	ENSP00000352035.2:p.Met648Ile
ENST00000637193.1:c.1341G>T	ENSP00000490734.1:p.Met447Ile
ENST00000344462.8:c.1851G>T	ENSP00000339611.4:p.Met617Ile
ENST00000357249.6:c.1512G>T	ENSP00000349789.3:p.Met504Ile
ENST00000359125.6:c.1944G>T	ENSP00000352035.2:p.Met648Ile
ENST00000360480.7:c.1860G>T	ENSP00000353668.3:p.Met620Ile
ENST00000370224.5:c.1968G>T	ENSP00000359244.2:p.Met656Ile
ENST00000625514.2:c.1932G>T	ENSP00000486040.1:p.Met644Ile
ENST00000626839.2:c.1890G>T	ENSP00000486706.1:p.Met630Ile
ENST00000629241.2:c.1860G>T	ENSP00000487142.1:p.Met620Ile
ENST00000629676.2:c.1679+6131G>T	ENSP00000486194.1:n.1679+6131G>T
NM_004518.4:c.1860G>T	NP_004509.2:p.Met620Ile
NM_172106.1:c.1890G>T	NP_742104.1:p.Met630Ile
NM_172107.2:c.1944G>T	NP_742105.1:p.Met648Ile
NM_172108.3:c.1851G>T	NP_742106.1:p.Met617Ile
XM_006723787.1:c.1986G>T	XP_006723850.1:p.Met662Ile
XM_011528807.1:c.2052G>T	XP_011527109.1:p.Met684Ile
XM_011528808.1:c.2049G>T	XP_011527110.1:p.Met683Ile
XM_011528809.1:c.2022G>T	XP_011527111.1:p.Met674Ile
XM_011528810.1:c.1998G>T	XP_011527112.1:p.Met666Ile
XM_011528811.1:c.1968G>T	XP_011527113.1:p.Met656Ile
XM_011528812.1:c.1941G>T	XP_011527114.1:p.Met647Ile
XM_011528813.1:c.1926G>T	XP_011527115.1:p.Met642Ile
XM_011528814.1:c.1533G>T	XP_011527116.1:p.Met511Ile
NM_004518.5:c.1860G>T	NP_004509.2:p.Met620Ile
NM_172106.2:c.1890G>T	NP_742104.1:p.Met630Ile
NM_172107.3:c.1944G>T	NP_742105.1:p.Met648Ile
NM_172108.4:c.1851G>T	NP_742106.1:p.Met617Ile
XM_011528810.2:c.1998G>T	XP_011527112.1:p.Met666Ile
XM_011528811.2:c.1968G>T	XP_011527113.1:p.Met656Ile
XM_017027841.2:c.1995G>T	XP_016883330.1:p.Met665Ile
XM_017027842.2:c.1932G>T	XP_016883331.1:p.Met644Ile
XM_017027843.1:c.1929G>T	XP_016883332.1:p.Met643Ile
XM_017027844.2:c.1887G>T	XP_016883333.1:p.Met629Ile
XM_017027845.1:c.960G>T	XP_016883334.1:p.Met320Ile
NM_004518.6:c.1860G>T	NP_004509.2:p.Met620Ile
NM_172106.3:c.1890G>T	NP_742104.1:p.Met630Ile
NM_172107.4:c.1944G>T MANE Select	NP_742105.1:p.Met648Ile
NM_172108.5:c.1851G>T	NP_742106.1:p.Met617Ile
NM_001382235.1:c.1998G>T	NP_001369164.1:p.Met666Ile