Canonical Allele Identifier: CA1202156632

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041354_160041356delinsGAA , CM000663.2:g.160041354_160041356delinsGAA	GRCh38
NC_000001.10:g.160011144_160011146delinsGAA , CM000663.1:g.160011144_160011146delinsGAA	GRCh37
NC_000001.9:g.158277768_158277770delinsGAA	NCBI36
NG_016411.1:g.33816_33818delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+478_671+480delinsTTC
ENST00000636689.1:n.95-2008_95-2006delinsTTC
ENST00000637644.1:c.487+690_487+692delinsTTC	ENSP00000490282.1:n.487+690_487+692delinsTTC
ENST00000638728.1:c.*37_*39delinsTTC	ENSP00000492619.1:n.*37_*39delinsTTC
ENST00000638840.1:c.899_901delinsTTC
ENST00000638868.1:c.*37_*39delinsTTC	ENSP00000491250.1:n.*37_*39delinsTTC
ENST00000639408.1:c.487+690_487+692delinsTTC	ENSP00000491635.1:n.487+690_487+692delinsTTC
ENST00000640017.1:c.669+478_669+480delinsTTC	ENSP00000491337.1:n.669+478_669+480delinsTTC
ENST00000640914.1:c.124+478_124+480delinsTTC
ENST00000644903.1:c.*37_*39delinsTTC MANE Select	ENSP00000495557.1:n.*37_*39delinsTTC
ENST00000368089.3:c.*37_*39delinsTTC	ENSP00000357068.3:n.*37_*39delinsTTC
ENST00000509700.1:n.462+478_462+480delinsTTC
NM_002241.4:c.*37_*39delinsTTC	NP_002232.2:n.*37_*39delinsTTC
NM_002241.5:c.*37_*39delinsTTC MANE Select	NP_002232.2:n.*37_*39delinsTTC