Canonical Allele Identifier: CA1164553130

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40838474C= , CM000663.2:g.40838474C=	GRCh38
NC_000001.10:g.41304146C= , CM000663.1:g.41304146C=	GRCh37
NC_000001.9:g.41076733C=	NCBI36
NG_008139.1:g.59463C=
NG_008139.2:g.59463C=
NG_008139.3:g.59688C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.2039C= MANE Select	ENSP00000262916.6:p.Ser680=
ENST00000347132.9:c.2039C=	ENSP00000262916.6:p.Ser680=
ENST00000443478.3:c.1620C=
ENST00000506017.1:n.1358C=
ENST00000509682.6:c.1877C=	ENSP00000423756.2:p.Ser626=
NM_004700.3:c.2039C=	NP_004691.2:p.Ser680=
NM_172163.2:c.1877C=	NP_751895.1:p.Ser626=
XM_017002792.1:c.1022C=	XP_016858281.1:p.Ser341=
NM_004700.4:c.2039C= MANE Select	NP_004691.2:p.Ser680=
NM_172163.3:c.1877C=	NP_751895.1:p.Ser626=