Canonical Allele Identifier: CA2366061669
Gene: KCNS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45093195G= , CM000682.2:g.45093195G= GRCh38
NC_000020.10:g.43721836G= , CM000682.1:g.43721836G= GRCh37
NC_000020.9:g.43155250G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537075.3:c.*1675C= MANE Select ENSP00000445595.1:n.*1675C=
ENST00000306117.5:c.*1675C= ENSP00000307694.1:n.*1675C=
NM_002251.3:c.*1675C= NP_002242.2:n.*1675C=
XM_005260409.3:c.*1675C= XP_005260466.1:n.*1675C=
NM_001322799.1:c.*1675C= NP_001309728.1:n.*1675C=
NM_002251.4:c.*1675C= NP_002242.2:n.*1675C=
XM_017027846.1:c.*1675C= XP_016883335.1:n.*1675C=
NM_001322799.2:c.*1675C= MANE Select NP_001309728.1:n.*1675C=
NM_002251.5:c.*1675C= NP_002242.2:n.*1675C=