Canonical Allele Identifier: CA2008285785

Gene: KCNJ1

Linked Data

• dbSNP Id: rs1943214980
• gnomAD v4: 11-128838933-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128838933G>T , CM000673.2:g.128838933G>T	GRCh38
NC_000011.9:g.128708828G>T , CM000673.1:g.128708828G>T	GRCh37
NC_000011.8:g.128214038G>T	NCBI36
NG_009379.1:g.33441C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.*192C>A MANE Select	ENSP00000376434.1:n.*192C>A
ENST00000324036.7:c.*192C>A	ENSP00000316233.3:n.*192C>A
ENST00000392664.2:c.*192C>A	ENSP00000376432.2:n.*192C>A
ENST00000392665.6:c.*192C>A	ENSP00000376433.2:n.*192C>A
ENST00000392666.5:c.*192C>A	ENSP00000376434.1:n.*192C>A
ENST00000440599.6:c.*192C>A	ENSP00000406320.2:n.*192C>A
NM_000220.4:c.*192C>A	NP_000211.1:n.*192C>A
NM_153764.2:c.*192C>A	NP_722448.1:n.*192C>A
NM_153765.2:c.*192C>A	NP_722449.3:n.*192C>A
NM_153766.2:c.*192C>A	NP_722450.1:n.*192C>A
NM_153767.3:c.*192C>A	NP_722451.1:n.*192C>A
NM_000220.6:c.*192C>A	NP_000211.1:n.*192C>A
NM_153764.3:c.*192C>A	NP_722448.1:n.*192C>A
NM_153765.3:c.*192C>A	NP_722449.3:n.*192C>A
NM_153766.3:c.*192C>A MANE Select	NP_722450.1:n.*192C>A
NM_153767.4:c.*192C>A	NP_722451.1:n.*192C>A