Canonical Allele Identifier: CA1982893275
Community Standard Title: NM_005472.5(KCNE3):c.198T= (p.Phe66=)
Gene: KCNE3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74457366A= , CM000673.2:g.74457366A= GRCh38
NC_000011.9:g.74168411A= , CM000673.1:g.74168411A= GRCh37
NC_000011.8:g.73846059A= NCBI36
NG_011833.1:g.15190T= , LRG_439:g.15190T=

Transcript Alleles

HGVS Amino-acid Change
NM_005472.5:c.198T= MANE Select NP_005463.1:p.Phe66=
ENST00000310128.9:c.198T= MANE Select ENSP00000310557.4:p.Phe66=
NM_005472.4:c.198T= , LRG_439t1:c.198T= NP_005463.1:p.Phe66=
ENST00000310128.8:c.198T= ENSP00000310557.4:p.Phe66=
ENST00000525550.1:c.198T= ENSP00000433633.1:p.Phe66=
ENST00000532569.5:c.198T= ENSP00000431739.1:p.Phe66=
XM_011544713.1:c.330T= XP_011543015.1:p.Phe110=
XM_011544713.2:c.330T= XP_011543015.1:p.Phe110=
XM_017017047.1:c.198T= XP_016872536.1:p.Phe66=
XM_017017048.1:c.198T= XP_016872537.1:p.Phe66=
XM_017017049.1:c.198T= XP_016872538.1:p.Phe66=
XM_017017051.2:c.198T= XP_016872540.1:p.Phe66=
XM_017017052.1:c.198T= XP_016872541.1:p.Phe66=