Canonical Allele Identifier: CA16078848
Gene: KCNK2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215107880C>G , CM000663.2:g.215107880C>G GRCh38
NC_000001.10:g.215281223C>G , CM000663.1:g.215281223C>G GRCh37
NC_000001.9:g.213347846C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000444842.7:c.358-16753C>G MANE Select ENSP00000394033.2:n.358-16753C>G
ENST00000391894.6:c.313-16753C>G ENSP00000375764.2:n.313-16753C>G
ENST00000391895.6:c.346-16753C>G ENSP00000375765.2:n.346-16753C>G
ENST00000444842.6:c.358-16753C>G ENSP00000394033.2:n.358-16753C>G
ENST00000457122.1:c.190-16753C>G ENSP00000413460.1:n.190-16753C>G
ENST00000467031.5:c.346-16753C>G ENSP00000420203.1:n.346-16753C>G
ENST00000470177.5:c.357+21202C>G ENSP00000419633.1:n.357+21202C>G
ENST00000474771.5:c.313-16753C>G ENSP00000420499.1:n.313-16753C>G
ENST00000478774.5:c.190-16753C>G ENSP00000420569.1:n.190-16753C>G
ENST00000486921.5:c.345+21202C>G ENSP00000418706.1:n.345+21202C>G
NM_001017424.2:c.346-16753C>G NP_001017424.1:n.346-16753C>G
NM_001017425.2:c.358-16753C>G NP_001017425.2:n.358-16753C>G
NM_014217.3:c.313-16753C>G NP_055032.1:n.313-16753C>G
XM_011509521.1:c.316-16753C>G XP_011507823.1:n.316-16753C>G
XM_011509522.1:c.190-16753C>G XP_011507824.1:n.190-16753C>G
XM_011509523.1:c.190-16753C>G XP_011507825.1:n.190-16753C>G
XM_011509524.1:c.190-16753C>G XP_011507826.1:n.190-16753C>G
XM_011509522.2:c.190-16753C>G XP_011507824.1:n.190-16753C>G
XM_011509524.2:c.190-16753C>G XP_011507826.1:n.190-16753C>G
XM_017001248.1:c.346-16753C>G XP_016856737.1:n.346-16753C>G
XM_017001249.1:c.316-16753C>G XP_016856738.1:n.316-16753C>G
NM_001017424.3:c.346-16753C>G NP_001017424.1:n.346-16753C>G
NM_001017425.3:c.358-16753C>G MANE Select NP_001017425.2:n.358-16753C>G
NM_014217.4:c.313-16753C>G NP_055032.1:n.313-16753C>G
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