Canonical Allele Identifier: CA2387126050

Gene: KCNE1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34507614T= , CM000683.2:g.34507614T=	GRCh38
NC_000021.8:g.35879912T= , CM000683.1:g.35879912T=	GRCh37
NC_000021.7:g.34801782T=	NCBI36
NG_009091.1:g.8702A= , LRG_290:g.8702A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683028.1:n.403-1856A=
ENST00000683564.1:n.403+3487A=
ENST00000684073.1:n.404-1856A=
ENST00000684327.1:n.403+3487A=
ENST00000684616.1:n.465-1856A=
ENST00000399286.3:c.-162+3487A= MANE Select	ENSP00000382226.2:n.-162+3487A=
ENST00000337385.7:c.-162+3487A=	ENSP00000337255.3:n.-162+3487A=
ENST00000399284.1:c.-134+3487A=	ENSP00000382225.1:n.-134+3487A=
ENST00000399286.2:c.-162+3487A=	ENSP00000382226.2:n.-162+3487A=
ENST00000611936.1:c.-51+3487A=	ENSP00000478215.1:n.-51+3487A=
NM_000219.5:c.-162+3487A=	NP_000210.2:n.-162+3487A=
NM_001270402.2:c.-162+3487A=	NP_001257331.1:n.-162+3487A=
NM_001270403.2:c.-134+3487A=	NP_001257332.1:n.-134+3487A=
NM_001270404.2:c.-51+3487A=	NP_001257333.1:n.-51+3487A=
XM_011529557.1:c.168+3487A=	XP_011527859.1:n.168+3487A=
NM_000219.6:c.-162+3487A= MANE Select	NP_000210.2:n.-162+3487A=
NM_001270402.3:c.-162+3487A=	NP_001257331.1:n.-162+3487A=
NM_001270404.3:c.-51+3487A=	NP_001257333.1:n.-51+3487A=