Canonical Allele Identifier: CA3003290442

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388028_17388029insGTC , CM000673.2:g.17388028_17388029insGTC	GRCh38
NC_000011.9:g.17409575_17409576insGTC , CM000673.1:g.17409575_17409576insGTC	GRCh37
NC_000011.8:g.17366151_17366152insGTC	NCBI36
NG_012446.1:g.5632_5633insACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.-165_-164insACG	ENSP00000436479.2:n.-165_-164insACG
ENST00000682350.1:c.-16-182_-16-181insACG	ENSP00000508090.1:n.-16-182_-16-181insACG
ENST00000682764.1:c.-16-182_-16-181insACG	ENSP00000506780.1:n.-16-182_-16-181insACG
ENST00000339994.5:c.64_65insACG MANE Select	ENSP00000345708.4:p.Pro21_Ala22insAsp
ENST00000339994.4:c.64_65insACG	ENSP00000345708.4:p.Pro21_Ala22insAsp
ENST00000526912.1:c.-27_-26insACG	ENSP00000432729.1:n.-27_-26insACG
ENST00000528731.1:c.-16-182_-16-181insACG	ENSP00000434755.1:n.-16-182_-16-181insACG
ENST00000528992.1:c.81_82insACG
NM_000525.3:c.64_65insACG	NP_000516.3:p.Pro21_Ala22insAsp
NM_001166290.1:c.-16-182_-16-181insACG	NP_001159762.1:n.-16-182_-16-181insACG
XM_006718226.2:c.-16-182_-16-181insACG	XP_006718289.1:n.-16-182_-16-181insACG
XR_930867.1:n.222_223insACG
XM_006718226.3:c.-16-182_-16-181insACG	XP_006718289.1:n.-16-182_-16-181insACG
XM_017017680.1:c.-16-182_-16-181insACG	XP_016873169.1:n.-16-182_-16-181insACG
NM_001166290.2:c.-16-182_-16-181insACG	NP_001159762.1:n.-16-182_-16-181insACG
NM_001377296.1:c.-27_-26insACG	NP_001364225.1:n.-27_-26insACG
NM_001377297.1:c.-16-182_-16-181insACG	NP_001364226.1:n.-16-182_-16-181insACG
NM_000525.4:c.64_65insACG MANE Select	NP_000516.3:p.Pro21_Ala22insAsp