Canonical Allele Identifier: CA2612638262

Gene: KCNJ11

Linked Data

• gnomAD v4: 11-17386890-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386890C>A , CM000673.2:g.17386890C>A	GRCh38
NC_000011.9:g.17408437C>A , CM000673.1:g.17408437C>A	GRCh37
NC_000011.8:g.17365013C>A	NCBI36
NG_012446.1:g.6770G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682350.1:c.*29G>T	ENSP00000508090.1:n.*29G>T
ENST00000682764.1:c.*29G>T	ENSP00000506780.1:n.*29G>T
ENST00000339994.5:c.*29G>T MANE Select	ENSP00000345708.4:n.*29G>T
ENST00000339994.4:c.*29G>T	ENSP00000345708.4:n.*29G>T
ENST00000528731.1:c.*29G>T	ENSP00000434755.1:n.*29G>T
NM_000525.3:c.*29G>T	NP_000516.3:n.*29G>T
NM_001166290.1:c.*29G>T	NP_001159762.1:n.*29G>T
XM_006718226.2:c.*29G>T	XP_006718289.1:n.*29G>T
XR_930867.1:n.1360G>T
XM_006718226.3:c.*29G>T	XP_006718289.1:n.*29G>T
XM_017017680.1:c.*29G>T	XP_016873169.1:n.*29G>T
NM_001166290.2:c.*29G>T	NP_001159762.1:n.*29G>T
NM_001377296.1:c.*29G>T	NP_001364225.1:n.*29G>T
NM_001377297.1:c.*29G>T	NP_001364226.1:n.*29G>T
NM_000525.4:c.*29G>T MANE Select	NP_000516.3:n.*29G>T