Canonical Allele Identifier: CA2841227753
Gene: KCNJ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128839393dup , CM000673.2:g.128839393dup GRCh38
NC_000011.9:g.128709288dup , CM000673.1:g.128709288dup GRCh37
NC_000011.8:g.128214498dup NCBI36
NG_009379.1:g.32982dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000392666.6:c.852dup MANE Select ENSP00000376434.1:p.Thr285HisfsTer?
ENST00000324036.7:c.852dup ENSP00000316233.3:p.Thr285HisfsTer?
ENST00000392664.2:c.909dup ENSP00000376432.2:p.Thr304HisfsTer?
ENST00000392665.6:c.852dup ENSP00000376433.2:p.Thr285HisfsTer?
ENST00000392666.5:c.852dup ENSP00000376434.1:p.Thr285HisfsTer?
ENST00000440599.6:c.852dup ENSP00000406320.2:p.Thr285HisfsTer?
NM_000220.4:c.909dup NP_000211.1:p.Thr304HisfsTer?
NM_153764.2:c.852dup NP_722448.1:p.Thr285HisfsTer?
NM_153765.2:c.903dup NP_722449.3:p.Thr302HisfsTer?
NM_153766.2:c.852dup NP_722450.1:p.Thr285HisfsTer?
NM_153767.3:c.852dup NP_722451.1:p.Thr285HisfsTer?
NM_000220.6:c.909dup NP_000211.1:p.Thr304HisfsTer?
NM_153764.3:c.852dup NP_722448.1:p.Thr285HisfsTer?
NM_153765.3:c.903dup NP_722449.3:p.Thr302HisfsTer?
NM_153766.3:c.852dup MANE Select NP_722450.1:p.Thr285HisfsTer?
NM_153767.4:c.852dup NP_722451.1:p.Thr285HisfsTer?