Canonical Allele Identifier: CA2008286599

Gene: KCNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839506_128839507delinsTG , CM000673.2:g.128839506_128839507delinsTG	GRCh38
NC_000011.9:g.128709401_128709402delinsTG , CM000673.1:g.128709401_128709402delinsTG	GRCh37
NC_000011.8:g.128214611_128214612delinsTG	NCBI36
NG_009379.1:g.32867_32868delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.737_738delinsCA MANE Select	ENSP00000376434.1:p.Pro246=
ENST00000324036.7:c.737_738delinsCA	ENSP00000316233.3:p.Pro246=
ENST00000392664.2:c.794_795delinsCA	ENSP00000376432.2:p.Pro265=
ENST00000392665.6:c.737_738delinsCA	ENSP00000376433.2:p.Pro246=
ENST00000392666.5:c.737_738delinsCA	ENSP00000376434.1:p.Pro246=
ENST00000440599.6:c.737_738delinsCA	ENSP00000406320.2:p.Pro246=
NM_000220.4:c.794_795delinsCA	NP_000211.1:p.Pro265=
NM_153764.2:c.737_738delinsCA	NP_722448.1:p.Pro246=
NM_153765.2:c.788_789delinsCA	NP_722449.3:p.Pro263=
NM_153766.2:c.737_738delinsCA	NP_722450.1:p.Pro246=
NM_153767.3:c.737_738delinsCA	NP_722451.1:p.Pro246=
NM_000220.6:c.794_795delinsCA	NP_000211.1:p.Pro265=
NM_153764.3:c.737_738delinsCA	NP_722448.1:p.Pro246=
NM_153765.3:c.788_789delinsCA	NP_722449.3:p.Pro263=
NM_153766.3:c.737_738delinsCA MANE Select	NP_722450.1:p.Pro246=
NM_153767.4:c.737_738delinsCA	NP_722451.1:p.Pro246=