Canonical Allele Identifier: CA2590193775
Gene: KCNE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34507707C>T , CM000683.2:g.34507707C>T GRCh38
NC_000021.8:g.35880005C>T , CM000683.1:g.35880005C>T GRCh37
NC_000021.7:g.34801875C>T NCBI36
NG_009091.1:g.8609G>A , LRG_290:g.8609G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000683028.1:n.403-1949G>A
ENST00000683564.1:n.403+3394G>A
ENST00000684073.1:n.404-1949G>A
ENST00000684327.1:n.403+3394G>A
ENST00000684616.1:n.465-1949G>A
ENST00000399286.3:c.-162+3394G>A MANE Select ENSP00000382226.2:n.-162+3394G>A
ENST00000337385.7:c.-162+3394G>A ENSP00000337255.3:n.-162+3394G>A
ENST00000399284.1:c.-134+3394G>A ENSP00000382225.1:n.-134+3394G>A
ENST00000399286.2:c.-162+3394G>A ENSP00000382226.2:n.-162+3394G>A
ENST00000611936.1:c.-51+3394G>A ENSP00000478215.1:n.-51+3394G>A
NM_000219.5:c.-162+3394G>A NP_000210.2:n.-162+3394G>A
NM_001270402.2:c.-162+3394G>A NP_001257331.1:n.-162+3394G>A
NM_001270403.2:c.-134+3394G>A NP_001257332.1:n.-134+3394G>A
NM_001270404.2:c.-51+3394G>A NP_001257333.1:n.-51+3394G>A
XM_011529557.1:c.168+3394G>A XP_011527859.1:n.168+3394G>A
NM_000219.6:c.-162+3394G>A MANE Select NP_000210.2:n.-162+3394G>A
NM_001270402.3:c.-162+3394G>A NP_001257331.1:n.-162+3394G>A
NM_001270404.3:c.-51+3394G>A NP_001257333.1:n.-51+3394G>A