Canonical Allele Identifier: CA2387127711

Gene: KCNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34511219T= , CM000683.2:g.34511219T=	GRCh38
NC_000021.8:g.35883517T= , CM000683.1:g.35883517T=	GRCh37
NC_000021.7:g.34805387T=	NCBI36
NG_009091.1:g.5097A= , LRG_290:g.5097A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682732.1:n.853A=
ENST00000683028.1:n.284A=
ENST00000683564.1:n.285A=
ENST00000684073.1:n.285A=
ENST00000684114.1:c.777A=
ENST00000684327.1:n.285A=
ENST00000684541.1:c.*266A=	ENSP00000508287.1:n.*266A=
ENST00000684616.1:n.346A=
ENST00000399286.3:c.-280A= MANE Select	ENSP00000382226.2:n.-280A=
ENST00000337385.7:c.-280A=	ENSP00000337255.3:n.-280A=
ENST00000399284.1:c.-252A=	ENSP00000382225.1:n.-252A=
ENST00000399286.2:c.-280A=	ENSP00000382226.2:n.-280A=
ENST00000489175.1:n.278A=
ENST00000611936.1:c.-169A=	ENSP00000478215.1:n.-169A=
NM_000219.5:c.-280A=	NP_000210.2:n.-280A=
NM_001270402.2:c.-280A=	NP_001257331.1:n.-280A=
NM_001270403.2:c.-252A=	NP_001257332.1:n.-252A=
NM_001270404.2:c.-169A=	NP_001257333.1:n.-169A=
XM_011529557.1:c.50A=	XP_011527859.1:p.Asp17=
NM_000219.6:c.-280A= MANE Select	NP_000210.2:n.-280A=
NM_001270402.3:c.-280A=	NP_001257331.1:n.-280A=
NM_001270404.3:c.-169A=	NP_001257333.1:n.-169A=