Canonical Allele Identifier: CA2653024193
Gene: KCNS1 HGNC NCBI

Linked Data

gnomAD v4: 20-45092879-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45092879T>C , CM000682.2:g.45092879T>C GRCh38
NC_000020.10:g.43721520T>C , CM000682.1:g.43721520T>C GRCh37
NC_000020.9:g.43154934T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537075.3:c.*1991A>G MANE Select ENSP00000445595.1:n.*1991A>G
ENST00000306117.5:c.*1991A>G ENSP00000307694.1:n.*1991A>G
NM_002251.3:c.*1991A>G NP_002242.2:n.*1991A>G
XM_005260409.3:c.*1991A>G XP_005260466.1:n.*1991A>G
NM_001322799.1:c.*1991A>G NP_001309728.1:n.*1991A>G
NM_002251.4:c.*1991A>G NP_002242.2:n.*1991A>G
XM_017027846.1:c.*1991A>G XP_016883335.1:n.*1991A>G
NM_001322799.2:c.*1991A>G MANE Select NP_001309728.1:n.*1991A>G
NM_002251.5:c.*1991A>G NP_002242.2:n.*1991A>G
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