Canonical Allele Identifier: CA320425715
Gene: KCNE1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2236609
MyVariant Identifiers: chr21:g.34449813A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34449813A>G , CM000683.2:g.34449813A>G GRCh38
NG_009091.1:g.66503T>C , LRG_290:g.66503T>C

Transcript Alleles

HGVS Amino-acid change
NM_000219.5:c.-50-129T>C VV NP_000210.2:p.=
NM_001127668.3:c.-50-129T>C VV NP_001121140.1:p.=
NM_001127669.3:c.-50-129T>C VV NP_001121141.1:p.=
NM_001127670.3:c.-50-129T>C VV NP_001121142.1:p.=
NM_001270402.2:c.-50-129T>C VV NP_001257331.1:p.=
NM_001270403.2:c.-50-129T>C VV NP_001257332.1:p.=
NM_001270404.2:c.-50-129T>C VV NP_001257333.1:p.=
NM_001270405.2:c.-50-129T>C VV NP_001257334.1:p.=
XM_011529555.1:c.13+5573T>C XP_011527857.1:p.=
XM_011529557.1:c.279+8841T>C XP_011527859.1:p.=
XM_017028342.1:c.14-129T>C XP_016883831.1:p.=
NM_000219.6:c.-50-129T>C VV MANE Preferred NP_000210.2:p.=
ENST00000337385.7:c.-50-129T>C ENSP00000337255.3:p.=
ENST00000399284.1:c.-50-129T>C ENSP00000382225.1:p.=
ENST00000399286.2:c.-50-129T>C ENSP00000382226.2:p.=
ENST00000399289.7:c.-50-129T>C ENSP00000382228.3:p.=
ENST00000416357.6:c.-50-129T>C ENSP00000416258.2:p.=
ENST00000432085.5:c.-50-129T>C ENSP00000412498.1:p.=
ENST00000611936.1:c.-50-129T>C ENSP00000478215.1:p.=
ENST00000621601.4:c.-50-129T>C ENSP00000483895.1:p.=