Canonical Allele Identifier: CA2387115563
Gene: KCNE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34458653C= , CM000683.2:g.34458653C= GRCh38
NG_009091.1:g.57663G= , LRG_290:g.57663G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399286.3:c.-51+1G= MANE Select ENSP00000382226.2:n.-51+1G=
ENST00000337385.7:c.-51+1G= ENSP00000337255.3:n.-51+1G=
ENST00000399284.1:c.-51+1G= ENSP00000382225.1:n.-51+1G=
ENST00000399286.2:c.-51+1G= ENSP00000382226.2:n.-51+1G=
ENST00000399289.7:c.-51+1G= ENSP00000382228.3:n.-51+1G=
ENST00000432085.5:c.-51+1G= ENSP00000412498.1:n.-51+1G=
ENST00000611936.1:c.-50-8969G= ENSP00000478215.1:n.-50-8969G=
ENST00000621601.4:c.-51+1G= ENSP00000483895.1:n.-51+1G=
NM_000219.5:c.-51+1G= NP_000210.2:n.-51+1G=
NM_001127668.3:c.-51+1G= NP_001121140.1:n.-51+1G=
NM_001127669.3:c.-51+1G= NP_001121141.1:n.-51+1G=
NM_001270402.2:c.-51+1G= NP_001257331.1:n.-51+1G=
NM_001270403.2:c.-51+1G= NP_001257332.1:n.-51+1G=
NM_001270404.2:c.-50-8969G= NP_001257333.1:n.-50-8969G=
NM_001270405.2:c.-51+1G= NP_001257334.1:n.-51+1G=
XM_011529557.1:c.279+1G= XP_011527859.1:n.279+1G=
NM_000219.6:c.-51+1G= MANE Select NP_000210.2:n.-51+1G=
NM_001127669.4:c.-51+1G= NP_001121141.1:n.-51+1G=
NM_001127668.4:c.-51+1G= NP_001121140.1:n.-51+1G=
NM_001270402.3:c.-51+1G= NP_001257331.1:n.-51+1G=
NM_001270404.3:c.-50-8969G= NP_001257333.1:n.-50-8969G=
NM_001270405.3:c.-51+1G= NP_001257334.1:n.-51+1G=