Canonical Allele Identifier: CA1141188918

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40819882T= , CM000663.2:g.40819882T=	GRCh38
NC_000001.10:g.41285554T= , CM000663.1:g.41285554T=	GRCh37
NC_000001.9:g.41058141T=	NCBI36
NG_008139.1:g.40871T=
NG_008139.2:g.40871T=
NG_008139.3:g.41096T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004700.4:c.842T= MANE Select	NP_004691.2:p.Leu281=
ENST00000347132.10:c.842T= MANE Select	ENSP00000262916.6:p.Leu281=
NM_004700.3:c.842T=	NP_004691.2:p.Leu281=
NM_172163.2:c.842T=	NP_751895.1:p.Leu281=
NM_172163.3:c.842T=	NP_751895.1:p.Leu281=
ENST00000347132.9:c.842T=	ENSP00000262916.6:p.Leu281=
ENST00000443478.3:c.528T=
ENST00000506017.1:n.161T=
ENST00000509682.6:c.842T=	ENSP00000423756.2:p.Leu281=
XM_011542417.1:c.842T=	XP_011540719.1:p.Leu281=
XM_011542418.1:c.842T=	XP_011540720.1:p.Leu281=
XM_011542419.1:c.842T=	XP_011540721.1:p.Leu281=
XM_011542420.1:c.842T=	XP_011540722.1:p.Leu281=
XM_017002792.1:c.-176T=	XP_016858281.1:n.-176T=
XR_946798.1:n.848T=
XR_946799.1:n.848T=
XR_946800.1:n.848T=