Canonical Allele Identifier: CA2008294777

Gene: KCNJ5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916368_128916371delinsGGAT , CM000673.2:g.128916368_128916371delinsGGAT	GRCh38
NC_000011.9:g.128786263_128786266delinsGGAT , CM000673.1:g.128786263_128786266delinsGGAT	GRCh37
NC_000011.8:g.128291473_128291476delinsGGAT	NCBI36
NG_023406.2:g.29951_29954delinsGGAT , LRG_333:g.29951_29954delinsGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.938-41_938-38delinsGGAT MANE Select	ENSP00000433295.1:n.938-41_938-38delinsGGAT
ENST00000338350.4:c.938-41_938-38delinsGGAT	ENSP00000339960.4:n.938-41_938-38delinsGGAT
ENST00000529694.5:c.938-41_938-38delinsGGAT	ENSP00000433295.1:n.938-41_938-38delinsGGAT
ENST00000533599.1:c.938-41_938-38delinsGGAT	ENSP00000434266.1:n.938-41_938-38delinsGGAT
NM_000890.3:c.938-41_938-38delinsGGAT , LRG_333t1:c.938-41_938-38delinsGGAT	NP_000881.3:n.938-41_938-38delinsGGAT
XM_011542809.1:c.938-41_938-38delinsGGAT	XP_011541111.1:n.938-41_938-38delinsGGAT
XM_011542810.1:c.938-41_938-38delinsGGAT	XP_011541112.1:n.938-41_938-38delinsGGAT
NM_000890.4:c.938-41_938-38delinsGGAT	NP_000881.3:n.938-41_938-38delinsGGAT
NM_001354169.1:c.938-41_938-38delinsGGAT	NP_001341098.1:n.938-41_938-38delinsGGAT
XM_011542809.2:c.938-41_938-38delinsGGAT	XP_011541111.1:n.938-41_938-38delinsGGAT
XM_011542810.3:c.938-41_938-38delinsGGAT	XP_011541112.1:n.938-41_938-38delinsGGAT
NM_000890.5:c.938-41_938-38delinsGGAT MANE Select	NP_000881.3:n.938-41_938-38delinsGGAT
NM_001354169.2:c.938-41_938-38delinsGGAT	NP_001341098.1:n.938-41_938-38delinsGGAT