Canonical Allele Identifier: CA4892594
Gene: KCNK9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1174840
ClinVar RCV Id: RCV001529008
dbSNP Id: rs2615374

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.139618747A>G , CM000670.2:g.139618747A>G GRCh38
NC_000008.10:g.140630990A>G , CM000670.1:g.140630990A>G GRCh37
NC_000008.9:g.140700172A>G NCBI36
NG_012842.2:g.89310T>C
NG_012842.3:g.89310T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000520439.3:c.636T>C MANE Select ENSP00000430676.1:p.Gly212=
ENST00000523477.2:n.460T>C
ENST00000647605.1:c.384T>C ENSP00000497893.1:p.Gly128=
ENST00000648164.1:c.636T>C ENSP00000498198.1:p.Gly212=
ENST00000648481.1:n.497T>C
ENST00000649473.1:c.600T>C ENSP00000498160.1:p.Gly200=
ENST00000649696.1:c.384T>C ENSP00000497127.1:p.Gly128=
ENST00000650269.1:c.636T>C ENSP00000496915.1:p.Gly212=
ENST00000303015.2:c.636T>C ENSP00000302166.1:p.Gly212=
ENST00000520439.1:c.636T>C ENSP00000430676.1:p.Gly212=
ENST00000522317.5:c.636T>C ENSP00000429847.1:p.Gly212=
NM_001282534.1:c.636T>C NP_001269463.1:p.Gly212=
NR_104210.1:n.700T>C
XM_011517101.1:c.636T>C XP_011515403.1:p.Gly212=
XM_011517102.1:c.636T>C XP_011515404.1:p.Gly212=
XM_011517103.1:c.306T>C XP_011515405.1:p.Gly102=
XM_011517101.2:c.636T>C XP_011515403.1:p.Gly212=
XM_011517102.2:c.636T>C XP_011515404.1:p.Gly212=
XM_011517103.2:c.306T>C XP_011515405.1:p.Gly102=
XM_017013530.1:c.306T>C XP_016869019.1:p.Gly102=
XM_017013531.1:c.306T>C XP_016869020.1:p.Gly102=
NM_001282534.2:c.636T>C MANE Select NP_001269463.1:p.Gly212=
NR_104210.2:n.767T>C