Canonical Allele Identifier: CA339895315

Gene: KCNQ4

Linked Data

• MyVariant Identifiers: chr1:g.41285019G>T (hg19) ; chr1:g.40819347G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40819347G>T , CM000663.2:g.40819347G>T	GRCh38
NC_000001.10:g.41285019G>T , CM000663.1:g.41285019G>T	GRCh37
NC_000001.9:g.41057606G>T	NCBI36
NG_008139.1:g.40336G>T
NG_008139.2:g.40336G>T
NG_008139.3:g.40561G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000347132.10:c.709G>T MANE Select	ENSP00000262916.6:p.Glu237Ter
ENST00000347132.9:c.709G>T	ENSP00000262916.6:p.Glu237Ter
ENST00000443478.3:c.395G>T
ENST00000506017.1:n.28G>T
ENST00000509682.6:c.709G>T	ENSP00000423756.2:p.Glu237Ter
NM_004700.3:c.709G>T	NP_004691.2:p.Glu237Ter
NM_172163.2:c.709G>T	NP_751895.1:p.Glu237Ter
XM_011542417.1:c.709G>T	XP_011540719.1:p.Glu237Ter
XM_011542418.1:c.709G>T	XP_011540720.1:p.Glu237Ter
XM_011542419.1:c.709G>T	XP_011540721.1:p.Glu237Ter
XM_011542420.1:c.709G>T	XP_011540722.1:p.Glu237Ter
XR_946798.1:n.715G>T
XR_946799.1:n.715G>T
XR_946800.1:n.715G>T
XM_017002792.1:c.-309G>T	XP_016858281.1:n.-309G>T
NM_004700.4:c.709G>T MANE Select	NP_004691.2:p.Glu237Ter
NM_172163.3:c.709G>T	NP_751895.1:p.Glu237Ter