Canonical Allele Identifier: CA2387099281
Gene: KCNE2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34370521T= , CM000683.2:g.34370521T= GRCh38
NC_000021.8:g.35742820T= , CM000683.1:g.35742820T= GRCh37
NC_000021.7:g.34664690T= NCBI36
NG_008804.1:g.11498T= , LRG_291:g.11498T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290310.4:c.43T= MANE Select ENSP00000290310.2:p.Phe15=
ENST00000290310.3:c.43T= ENSP00000290310.2:p.Phe15=
NM_172201.1:c.43T= , LRG_291t1:c.43T= NP_751951.1:p.Phe15=
XR_937683.1:n.800A=
XR_937684.1:n.800A=
XR_001755012.2:n.921A=
XR_001755013.2:n.800A=
XR_937683.2:n.800A=
NM_172201.2:c.43T= MANE Select NP_751951.1:p.Phe15=