Canonical Allele Identifier: CA1955119248

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387402C= , CM000673.2:g.17387402C=	GRCh38
NC_000011.9:g.17408949C= , CM000673.1:g.17408949C=	GRCh37
NC_000011.8:g.17365525C=	NCBI36
NG_012446.1:g.6258G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682350.1:c.429G=	ENSP00000508090.1:p.Val143=
ENST00000682764.1:c.429G=	ENSP00000506780.1:p.Val143=
ENST00000339994.5:c.690G= MANE Select	ENSP00000345708.4:p.Val230=
ENST00000339994.4:c.690G=	ENSP00000345708.4:p.Val230=
ENST00000526912.1:c.429G=	ENSP00000432729.1:p.Val143=
ENST00000528731.1:c.429G=	ENSP00000434755.1:p.Val143=
NM_000525.3:c.690G=	NP_000516.3:p.Val230=
NM_001166290.1:c.429G=	NP_001159762.1:p.Val143=
XM_006718226.2:c.429G=	XP_006718289.1:p.Val143=
XR_930867.1:n.848G=
XM_006718226.3:c.429G=	XP_006718289.1:p.Val143=
XM_017017680.1:c.429G=	XP_016873169.1:p.Val143=
NM_001166290.2:c.429G=	NP_001159762.1:p.Val143=
NM_001377296.1:c.429G=	NP_001364225.1:p.Val143=
NM_001377297.1:c.429G=	NP_001364226.1:p.Val143=
NM_000525.4:c.690G= MANE Select	NP_000516.3:p.Val230=