Canonical Allele Identifier: CA2366061680
Gene: KCNS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45093223C= , CM000682.2:g.45093223C= GRCh38
NC_000020.10:g.43721864C= , CM000682.1:g.43721864C= GRCh37
NC_000020.9:g.43155278C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537075.3:c.*1647G= MANE Select ENSP00000445595.1:n.*1647G=
ENST00000306117.5:c.*1647G= ENSP00000307694.1:n.*1647G=
NM_002251.3:c.*1647G= NP_002242.2:n.*1647G=
XM_005260409.3:c.*1647G= XP_005260466.1:n.*1647G=
NM_001322799.1:c.*1647G= NP_001309728.1:n.*1647G=
NM_002251.4:c.*1647G= NP_002242.2:n.*1647G=
XM_017027846.1:c.*1647G= XP_016883335.1:n.*1647G=
NM_001322799.2:c.*1647G= MANE Select NP_001309728.1:n.*1647G=
NM_002251.5:c.*1647G= NP_002242.2:n.*1647G=