Canonical Allele Identifier: CA16609476

Gene: KCNK9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.139618677C>G , CM000670.2:g.139618677C>G	GRCh38
NC_000008.10:g.140630920C>G , CM000670.1:g.140630920C>G	GRCh37
NC_000008.9:g.140700102C>G	NCBI36
NG_012842.2:g.89380G>C
NG_012842.3:g.89380G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001282534.2:c.706G>C MANE Select	NP_001269463.1:p.Gly236Arg
ENST00000520439.3:c.706G>C MANE Select	ENSP00000430676.1:p.Gly236Arg
NM_001282534.1:c.706G>C	NP_001269463.1:p.Gly236Arg
NR_104210.1:n.770G>C
NR_104210.2:n.837G>C
ENST00000303015.2:c.706G>C	ENSP00000302166.1:p.Gly236Arg
ENST00000520439.1:c.706G>C	ENSP00000430676.1:p.Gly236Arg
ENST00000522317.5:c.706G>C	ENSP00000429847.1:p.Gly236Arg
ENST00000523477.2:n.530G>C
ENST00000647605.1:c.454G>C	ENSP00000497893.1:p.Gly152Arg
ENST00000648164.1:c.706G>C	ENSP00000498198.1:p.Gly236Arg
ENST00000648481.1:n.567G>C
ENST00000649473.1:c.670G>C	ENSP00000498160.1:p.Gly224Arg
ENST00000649696.1:c.454G>C	ENSP00000497127.1:p.Gly152Arg
ENST00000650269.1:c.706G>C	ENSP00000496915.1:p.Gly236Arg
XM_011517101.1:c.706G>C	XP_011515403.1:p.Gly236Arg
XM_011517101.2:c.706G>C	XP_011515403.1:p.Gly236Arg
XM_011517102.1:c.706G>C	XP_011515404.1:p.Gly236Arg
XM_011517102.2:c.706G>C	XP_011515404.1:p.Gly236Arg
XM_011517103.1:c.376G>C	XP_011515405.1:p.Gly126Arg
XM_011517103.2:c.376G>C	XP_011515405.1:p.Gly126Arg
XM_017013530.1:c.376G>C	XP_016869019.1:p.Gly126Arg
XM_017013531.1:c.376G>C	XP_016869020.1:p.Gly126Arg