Canonical Allele Identifier: CA2387099388
Gene: KCNE2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370744T= , CM000683.2:g.34370744T= GRCh38
NC_000021.8:g.35743043T= , CM000683.1:g.35743043T= GRCh37
NC_000021.7:g.34664913T= NCBI36
NG_008804.1:g.11721T= , LRG_291:g.11721T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290310.4:c.266T= MANE Select ENSP00000290310.2:p.Val89=
ENST00000290310.3:c.266T= ENSP00000290310.2:p.Val89=
NM_172201.1:c.266T= , LRG_291t1:c.266T= NP_751951.1:p.Val89=
XR_937683.1:n.577A=
XR_937684.1:n.577A=
XR_001755012.2:n.698A=
XR_001755013.2:n.577A=
XR_937683.2:n.577A=
NM_172201.2:c.266T= MANE Select NP_751951.1:p.Val89=