Canonical Allele Identifier: CA379774177

Gene: KCNJ11

Linked Data

• MyVariant Identifiers: chr11:g.17409280G>A (hg19) ; chr11:g.17387733G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387733G>A , CM000673.2:g.17387733G>A	GRCh38
NC_000011.9:g.17409280G>A , CM000673.1:g.17409280G>A	GRCh37
NC_000011.8:g.17365856G>A	NCBI36
NG_012446.1:g.5927C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.131C>T	ENSP00000436479.2:p.Ala44Val
ENST00000682350.1:c.98C>T	ENSP00000508090.1:p.Ala33Val
ENST00000682764.1:c.98C>T	ENSP00000506780.1:p.Ala33Val
ENST00000339994.5:c.359C>T MANE Select	ENSP00000345708.4:p.Ala120Val
ENST00000339994.4:c.359C>T	ENSP00000345708.4:p.Ala120Val
ENST00000526912.1:c.98C>T	ENSP00000432729.1:p.Ala33Val
ENST00000528731.1:c.98C>T	ENSP00000434755.1:p.Ala33Val
ENST00000528992.1:c.376C>T
NM_000525.3:c.359C>T	NP_000516.3:p.Ala120Val
NM_001166290.1:c.98C>T	NP_001159762.1:p.Ala33Val
XM_006718226.2:c.98C>T	XP_006718289.1:p.Ala33Val
XR_930867.1:n.517C>T
XM_006718226.3:c.98C>T	XP_006718289.1:p.Ala33Val
XM_017017680.1:c.98C>T	XP_016873169.1:p.Ala33Val
NM_001166290.2:c.98C>T	NP_001159762.1:p.Ala33Val
NM_001377296.1:c.98C>T	NP_001364225.1:p.Ala33Val
NM_001377297.1:c.98C>T	NP_001364226.1:p.Ala33Val
NM_000525.4:c.359C>T MANE Select	NP_000516.3:p.Ala120Val