Canonical Allele Identifier: CA1220147155
Gene: KCNK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215152892G>T , CM000663.2:g.215152892G>T GRCh38
NC_000001.10:g.215326235G>T , CM000663.1:g.215326235G>T GRCh37
NC_000001.9:g.213392858G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000444842.7:c.476-16307G>T MANE Select ENSP00000394033.2:n.476-16307G>T
ENST00000391894.6:c.431-16307G>T ENSP00000375764.2:n.431-16307G>T
ENST00000391895.6:c.464-16307G>T ENSP00000375765.2:n.464-16307G>T
ENST00000444842.6:c.476-16307G>T ENSP00000394033.2:n.476-16307G>T
ENST00000457122.1:c.308-16307G>T ENSP00000413460.1:n.308-16307G>T
ENST00000467031.5:c.464-16307G>T ENSP00000420203.1:n.464-16307G>T
ENST00000470177.5:c.358-16307G>T ENSP00000419633.1:n.358-16307G>T
ENST00000474771.5:c.431-16307G>T ENSP00000420499.1:n.431-16307G>T
ENST00000478774.5:c.308-16307G>T ENSP00000420569.1:n.308-16307G>T
ENST00000486921.5:c.346-16307G>T ENSP00000418706.1:n.346-16307G>T
NM_001017424.2:c.464-16307G>T NP_001017424.1:n.464-16307G>T
NM_001017425.2:c.476-16307G>T NP_001017425.2:n.476-16307G>T
NM_014217.3:c.431-16307G>T NP_055032.1:n.431-16307G>T
XM_011509521.1:c.434-16307G>T XP_011507823.1:n.434-16307G>T
XM_011509522.1:c.308-16307G>T XP_011507824.1:n.308-16307G>T
XM_011509523.1:c.308-16307G>T XP_011507825.1:n.308-16307G>T
XM_011509524.1:c.308-16307G>T XP_011507826.1:n.308-16307G>T
XM_011509522.2:c.308-16307G>T XP_011507824.1:n.308-16307G>T
XM_011509524.2:c.308-16307G>T XP_011507826.1:n.308-16307G>T
XM_017001248.1:c.464-16307G>T XP_016856737.1:n.464-16307G>T
XM_017001249.1:c.434-16307G>T XP_016856738.1:n.434-16307G>T
NM_001017424.3:c.464-16307G>T NP_001017424.1:n.464-16307G>T
NM_001017425.3:c.476-16307G>T MANE Select NP_001017425.2:n.476-16307G>T
NM_014217.4:c.431-16307G>T NP_055032.1:n.431-16307G>T