Canonical Allele Identifier: CA10650385
Gene: KCNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 339735
dbSNP Id: rs886057015
MyVariant Identifiers: chr21:g.34447317A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34447317A>G , CM000683.2:g.34447317A>G GRCh38
NG_009091.1:g.68999T>C , LRG_290:g.68999T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399286.3:c.*1928T>C MANE Select ENSP00000382226.2:n.*1928T>C
ENST00000337385.7:c.*1928T>C ENSP00000337255.3:n.*1928T>C
ENST00000399289.7:c.*1928T>C ENSP00000382228.3:n.*1928T>C
ENST00000432085.5:c.*1928T>C ENSP00000412498.1:n.*1928T>C
ENST00000611936.1:c.*1928T>C ENSP00000478215.1:n.*1928T>C
ENST00000621601.4:c.*1928T>C ENSP00000483895.1:n.*1928T>C
NM_000219.5:c.*1928T>C NP_000210.2:n.*1928T>C
NM_001127668.3:c.*1928T>C NP_001121140.1:n.*1928T>C
NM_001127669.3:c.*1928T>C NP_001121141.1:n.*1928T>C
NM_001127670.3:c.*1928T>C NP_001121142.1:n.*1928T>C
NM_001270402.2:c.*1928T>C NP_001257331.1:n.*1928T>C
NM_001270403.2:c.*1928T>C NP_001257332.1:n.*1928T>C
NM_001270404.2:c.*1928T>C NP_001257333.1:n.*1928T>C
NM_001270405.2:c.*1928T>C NP_001257334.1:n.*1928T>C
XM_011529555.1:c.13+8069T>C XP_011527857.1:n.13+8069T>C
XM_011529557.1:c.279+11337T>C XP_011527859.1:n.279+11337T>C
XM_017028342.1:c.*1928T>C XP_016883831.1:n.*1928T>C
NM_000219.6:c.*1928T>C MANE Select NP_000210.2:n.*1928T>C
NM_001127669.4:c.*1928T>C NP_001121141.1:n.*1928T>C
NM_001127668.4:c.*1928T>C NP_001121140.1:n.*1928T>C
NM_001127670.4:c.*1928T>C NP_001121142.1:n.*1928T>C
NM_001270402.3:c.*1928T>C NP_001257331.1:n.*1928T>C
NM_001270404.3:c.*1928T>C NP_001257333.1:n.*1928T>C
NM_001270405.3:c.*1928T>C NP_001257334.1:n.*1928T>C