Canonical Allele Identifier: CA421597112

Gene: KCNJ10

Linked Data

• MyVariant Identifiers: chr1:g.160011336A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041546A>T , CM000663.2:g.160041546A>T	GRCh38
NC_000001.10:g.160011336A>T , CM000663.1:g.160011336A>T	GRCh37
NC_000001.9:g.158277960A>T	NCBI36
NG_016411.1:g.33626T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000509700.2:c.671+288T>A
ENST00000636689.1:n.95-2198T>A
ENST00000637644.1:c.487+500T>A	ENSP00000490282.1:n.487+500T>A
ENST00000638728.1:c.987T>A	ENSP00000492619.1:p.Leu329=
ENST00000638840.1:c.709T>A
ENST00000638868.1:c.987T>A	ENSP00000491250.1:p.Leu329=
ENST00000639408.1:c.487+500T>A	ENSP00000491635.1:n.487+500T>A
ENST00000640017.1:c.669+288T>A	ENSP00000491337.1:n.669+288T>A
ENST00000640914.1:c.124+288T>A
ENST00000644903.1:c.987T>A MANE Select	ENSP00000495557.1:p.Leu329=
ENST00000368089.3:c.987T>A	ENSP00000357068.3:p.Leu329=
ENST00000509700.1:n.462+288T>A
NM_002241.4:c.987T>A	NP_002232.2:p.Leu329=
NM_002241.5:c.987T>A MANE Select	NP_002232.2:p.Leu329=