Canonical Allele Identifier: CA2387127700

Gene: KCNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34511193C= , CM000683.2:g.34511193C=	GRCh38
NC_000021.8:g.35883491C= , CM000683.1:g.35883491C=	GRCh37
NC_000021.7:g.34805361C=	NCBI36
NG_009091.1:g.5123G= , LRG_290:g.5123G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682732.1:n.879G=
ENST00000683028.1:n.310G=
ENST00000683564.1:n.311G=
ENST00000684073.1:n.311G=
ENST00000684114.1:c.803G=
ENST00000684327.1:n.311G=
ENST00000684541.1:c.*292G=	ENSP00000508287.1:n.*292G=
ENST00000684616.1:n.372G=
ENST00000399286.3:c.-254G= MANE Select	ENSP00000382226.2:n.-254G=
ENST00000337385.7:c.-254G=	ENSP00000337255.3:n.-254G=
ENST00000399284.1:c.-226G=	ENSP00000382225.1:n.-226G=
ENST00000399286.2:c.-254G=	ENSP00000382226.2:n.-254G=
ENST00000489175.1:n.304G=
ENST00000611936.1:c.-143G=	ENSP00000478215.1:n.-143G=
NM_000219.5:c.-254G=	NP_000210.2:n.-254G=
NM_001270402.2:c.-254G=	NP_001257331.1:n.-254G=
NM_001270403.2:c.-226G=	NP_001257332.1:n.-226G=
NM_001270404.2:c.-143G=	NP_001257333.1:n.-143G=
XM_011529557.1:c.76G=	XP_011527859.1:p.Glu26=
NM_000219.6:c.-254G= MANE Select	NP_000210.2:n.-254G=
NM_001270402.3:c.-254G=	NP_001257331.1:n.-254G=
NM_001270404.3:c.-143G=	NP_001257333.1:n.-143G=