Canonical Allele Identifier: CA2366061519
Gene: KCNS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45092890A= , CM000682.2:g.45092890A= GRCh38
NC_000020.10:g.43721531A= , CM000682.1:g.43721531A= GRCh37
NC_000020.9:g.43154945A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537075.3:c.*1980T= MANE Select ENSP00000445595.1:n.*1980T=
ENST00000306117.5:c.*1980T= ENSP00000307694.1:n.*1980T=
NM_002251.3:c.*1980T= NP_002242.2:n.*1980T=
XM_005260409.3:c.*1980T= XP_005260466.1:n.*1980T=
NM_001322799.1:c.*1980T= NP_001309728.1:n.*1980T=
NM_002251.4:c.*1980T= NP_002242.2:n.*1980T=
XM_017027846.1:c.*1980T= XP_016883335.1:n.*1980T=
NM_001322799.2:c.*1980T= MANE Select NP_001309728.1:n.*1980T=
NM_002251.5:c.*1980T= NP_002242.2:n.*1980T=