Canonical Allele Identifier: CA1017880579
Gene: KCNS1 HGNC NCBI

Linked Data

dbSNP Id: rs1981039164

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45092777C>T , CM000682.2:g.45092777C>T GRCh38
NC_000020.10:g.43721418C>T , CM000682.1:g.43721418C>T GRCh37
NC_000020.9:g.43154832C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537075.3:c.*2093G>A MANE Select ENSP00000445595.1:n.*2093G>A
ENST00000306117.5:c.*2093G>A ENSP00000307694.1:n.*2093G>A
NM_002251.3:c.*2093G>A NP_002242.2:n.*2093G>A
XM_005260409.3:c.*2093G>A XP_005260466.1:n.*2093G>A
NM_001322799.1:c.*2093G>A NP_001309728.1:n.*2093G>A
NM_002251.4:c.*2093G>A NP_002242.2:n.*2093G>A
XM_017027846.1:c.*2093G>A XP_016883335.1:n.*2093G>A
NM_001322799.2:c.*2093G>A MANE Select NP_001309728.1:n.*2093G>A
NM_002251.5:c.*2093G>A NP_002242.2:n.*2093G>A