Canonical Allele Identifier: CA224975650
Gene: KCNE3 HGNC NCBI

Linked Data

dbSNP Id: rs1006962870

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74457290del , CM000673.2:g.74457290del GRCh38
NC_000011.9:g.74168335del , CM000673.1:g.74168335del GRCh37
NC_000011.8:g.73845983del NCBI36
NG_011833.1:g.15266del , LRG_439:g.15266del

Transcript Alleles

HGVS Amino-acid change
ENST00000310128.9:c.274del MANE Select ENSP00000310557.4:p.Tyr92IlefsTer11
ENST00000310128.8:c.274del ENSP00000310557.4:p.Tyr92IlefsTer11
ENST00000525550.1:c.274del ENSP00000433633.1:p.Tyr92IlefsTer11
ENST00000532569.5:c.274del ENSP00000431739.1:p.Tyr92IlefsTer?
NM_005472.4:c.274del , LRG_439t1:c.274del NP_005463.1:p.Tyr92IlefsTer11
XM_011544713.1:c.406del XP_011543015.1:p.Tyr136IlefsTer11
XM_011544713.2:c.406del XP_011543015.1:p.Tyr136IlefsTer11
XM_017017047.1:c.274del XP_016872536.1:p.Tyr92IlefsTer11
XM_017017048.1:c.274del XP_016872537.1:p.Tyr92IlefsTer11
XM_017017049.1:c.274del XP_016872538.1:p.Tyr92IlefsTer11
XM_017017051.2:c.274del XP_016872540.1:p.Tyr92IlefsTer11
XM_017017052.1:c.274del XP_016872541.1:p.Tyr92IlefsTer11
NM_005472.5:c.274del MANE Select NP_005463.1:p.Tyr92IlefsTer11