Canonical Allele Identifier: CA473515464

Gene: KCNJ11

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387528C>T , CM000673.2:g.17387528C>T	GRCh38
NC_000011.9:g.17409075C>T , CM000673.1:g.17409075C>T	GRCh37
NC_000011.8:g.17365651C>T	NCBI36
NG_012446.1:g.6132G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682350.1:c.303G>A	ENSP00000508090.1:p.Val101=
ENST00000682764.1:c.303G>A	ENSP00000506780.1:p.Val101=
ENST00000339994.5:c.564G>A MANE Select	ENSP00000345708.4:p.Val188=
ENST00000339994.4:c.564G>A	ENSP00000345708.4:p.Val188=
ENST00000526912.1:c.303G>A	ENSP00000432729.1:p.Val101=
ENST00000528731.1:c.303G>A	ENSP00000434755.1:p.Val101=
NM_000525.3:c.564G>A	NP_000516.3:p.Val188=
NM_001166290.1:c.303G>A	NP_001159762.1:p.Val101=
XM_006718226.2:c.303G>A	XP_006718289.1:p.Val101=
XR_930867.1:n.722G>A
XM_006718226.3:c.303G>A	XP_006718289.1:p.Val101=
XM_017017680.1:c.303G>A	XP_016873169.1:p.Val101=
NM_001166290.2:c.303G>A	NP_001159762.1:p.Val101=
NM_001377296.1:c.303G>A	NP_001364225.1:p.Val101=
NM_001377297.1:c.303G>A	NP_001364226.1:p.Val101=
NM_000525.4:c.564G>A MANE Select	NP_000516.3:p.Val188=