Canonical Allele Identifier: CA1164531212

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40784332A= , CM000663.2:g.40784332A=	GRCh38
NC_000001.10:g.41250004A= , CM000663.1:g.41250004A=	GRCh37
NC_000001.9:g.41022591A=	NCBI36
NG_008139.1:g.5321A=
NG_008139.2:g.5321A=
NG_008139.3:g.5546A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.239A= MANE Select	ENSP00000262916.6:p.Tyr80=
ENST00000347132.9:c.239A=	ENSP00000262916.6:p.Tyr80=
ENST00000509682.6:c.239A=	ENSP00000423756.2:p.Tyr80=
NM_004700.3:c.239A=	NP_004691.2:p.Tyr80=
NM_172163.2:c.239A=	NP_751895.1:p.Tyr80=
XM_011542417.1:c.239A=	XP_011540719.1:p.Tyr80=
XM_011542418.1:c.239A=	XP_011540720.1:p.Tyr80=
XM_011542419.1:c.239A=	XP_011540721.1:p.Tyr80=
XM_011542420.1:c.239A=	XP_011540722.1:p.Tyr80=
XR_946798.1:n.245A=
XR_946799.1:n.245A=
XR_946800.1:n.245A=
NM_004700.4:c.239A= MANE Select	NP_004691.2:p.Tyr80=
NM_172163.3:c.239A=	NP_751895.1:p.Tyr80=