Canonical Allele Identifier: CA2612640326

Gene: KCNJ11

Linked Data

• gnomAD v4: 11-17388198-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388198G>T , CM000673.2:g.17388198G>T	GRCh38
NC_000011.9:g.17409745G>T , CM000673.1:g.17409745G>T	GRCh37
NC_000011.8:g.17366321G>T	NCBI36
NG_012446.1:g.5462C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.-213-122C>A	ENSP00000436479.2:n.-213-122C>A
ENST00000682350.1:c.-16-352C>A	ENSP00000508090.1:n.-16-352C>A
ENST00000682764.1:c.-16-352C>A	ENSP00000506780.1:n.-16-352C>A
ENST00000339994.5:c.-107C>A MANE Select	ENSP00000345708.4:n.-107C>A
ENST00000339994.4:c.-107C>A	ENSP00000345708.4:n.-107C>A
ENST00000526912.1:c.-75-122C>A	ENSP00000432729.1:n.-75-122C>A
ENST00000528731.1:c.-16-352C>A	ENSP00000434755.1:n.-16-352C>A
ENST00000528992.1:c.33-122C>A
NM_000525.3:c.-107C>A	NP_000516.3:n.-107C>A
NM_001166290.1:c.-16-352C>A	NP_001159762.1:n.-16-352C>A
XM_006718226.2:c.-16-352C>A	XP_006718289.1:n.-16-352C>A
XR_930867.1:n.52C>A
XM_006718226.3:c.-16-352C>A	XP_006718289.1:n.-16-352C>A
XM_017017680.1:c.-16-352C>A	XP_016873169.1:n.-16-352C>A
NM_001166290.2:c.-16-352C>A	NP_001159762.1:n.-16-352C>A
NM_001377296.1:c.-75-122C>A	NP_001364225.1:n.-75-122C>A
NM_001377297.1:c.-16-352C>A	NP_001364226.1:n.-16-352C>A
NM_000525.4:c.-107C>A MANE Select	NP_000516.3:n.-107C>A