Canonical Allele Identifier: CA1139938700

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160039629A= , CM000663.2:g.160039629A=	GRCh38
NC_000001.10:g.160009419A= , CM000663.1:g.160009419A=	GRCh37
NC_000001.9:g.158276043A=	NCBI36
NG_016411.1:g.35543T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+2205T=
ENST00000636689.1:n.95-281T=
ENST00000637644.1:c.487+2417T=	ENSP00000490282.1:n.487+2417T=
ENST00000638728.1:c.*1764T=	ENSP00000492619.1:n.*1764T=
ENST00000638840.1:c.1892T=
ENST00000638868.1:c.*1764T=	ENSP00000491250.1:n.*1764T=
ENST00000639408.1:c.587+873T=	ENSP00000491635.1:n.587+873T=
ENST00000640017.1:c.1642T=	ENSP00000491337.1:n.1642T=
ENST00000640914.1:c.224+873T=
ENST00000644903.1:c.*1764T= MANE Select	ENSP00000495557.1:n.*1764T=
ENST00000368089.3:c.*1764T=	ENSP00000357068.3:n.*1764T=
NM_002241.4:c.*1764T=	NP_002232.2:n.*1764T=
NM_002241.5:c.*1764T= MANE Select	NP_002232.2:n.*1764T=