Canonical Allele Identifier: CA1982893235
Gene: KCNE3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74457266C= , CM000673.2:g.74457266C= GRCh38
NC_000011.9:g.74168311C= , CM000673.1:g.74168311C= GRCh37
NC_000011.8:g.73845959C= NCBI36
NG_011833.1:g.15290G= , LRG_439:g.15290G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310128.9:c.298G= MANE Select ENSP00000310557.4:p.Val100=
ENST00000310128.8:c.298G= ENSP00000310557.4:p.Val100=
ENST00000525550.1:c.298G= ENSP00000433633.1:p.Val100=
ENST00000532569.5:c.298G=
NM_005472.4:c.298G= , LRG_439t1:c.298G= NP_005463.1:p.Val100=
XM_011544713.1:c.430G= XP_011543015.1:p.Val144=
XM_011544713.2:c.430G= XP_011543015.1:p.Val144=
XM_017017047.1:c.298G= XP_016872536.1:p.Val100=
XM_017017048.1:c.298G= XP_016872537.1:p.Val100=
XM_017017049.1:c.298G= XP_016872538.1:p.Val100=
XM_017017051.2:c.298G= XP_016872540.1:p.Val100=
XM_017017052.1:c.298G= XP_016872541.1:p.Val100=
NM_005472.5:c.298G= MANE Select NP_005463.1:p.Val100=