Canonical Allele Identifier: CA1202156669

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041479G= , CM000663.2:g.160041479G=	GRCh38
NC_000001.10:g.160011269G= , CM000663.1:g.160011269G=	GRCh37
NC_000001.9:g.158277893G=	NCBI36
NG_016411.1:g.33693C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+355C=
ENST00000636689.1:n.95-2131C=
ENST00000637644.1:c.487+567C=	ENSP00000490282.1:n.487+567C=
ENST00000638728.1:c.1054C=	ENSP00000492619.1:p.Pro352=
ENST00000638840.1:c.776C=
ENST00000638868.1:c.1054C=	ENSP00000491250.1:p.Pro352=
ENST00000639408.1:c.487+567C=	ENSP00000491635.1:n.487+567C=
ENST00000640017.1:c.669+355C=	ENSP00000491337.1:n.669+355C=
ENST00000640914.1:c.124+355C=
ENST00000644903.1:c.1054C= MANE Select	ENSP00000495557.1:p.Pro352=
ENST00000368089.3:c.1054C=	ENSP00000357068.3:p.Pro352=
ENST00000509700.1:n.462+355C=
NM_002241.4:c.1054C=	NP_002232.2:p.Pro352=
NM_002241.5:c.1054C= MANE Select	NP_002232.2:p.Pro352=