Canonical Allele Identifier: CA1982893240
Gene: KCNE3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74457278T= , CM000673.2:g.74457278T= GRCh38
NC_000011.9:g.74168323T= , CM000673.1:g.74168323T= GRCh37
NC_000011.8:g.73845971T= NCBI36
NG_011833.1:g.15278A= , LRG_439:g.15278A=

Transcript Alleles

HGVS Amino-acid change
ENST00000310128.9:c.286A= MANE Select ENSP00000310557.4:p.Ile96=
ENST00000310128.8:c.286A= ENSP00000310557.4:p.Ile96=
ENST00000525550.1:c.286A= ENSP00000433633.1:p.Ile96=
ENST00000532569.5:c.286A= ENSP00000431739.1:p.Ile96=
NM_005472.4:c.286A= , LRG_439t1:c.286A= NP_005463.1:p.Ile96=
XM_011544713.1:c.418A= XP_011543015.1:p.Ile140=
XM_011544713.2:c.418A= XP_011543015.1:p.Ile140=
XM_017017047.1:c.286A= XP_016872536.1:p.Ile96=
XM_017017048.1:c.286A= XP_016872537.1:p.Ile96=
XM_017017049.1:c.286A= XP_016872538.1:p.Ile96=
XM_017017051.2:c.286A= XP_016872540.1:p.Ile96=
XM_017017052.1:c.286A= XP_016872541.1:p.Ile96=
NM_005472.5:c.286A= MANE Select NP_005463.1:p.Ile96=