Canonical Allele Identifier: CA1202155172
Gene: KCNJ10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160037475A= , CM000663.2:g.160037475A= GRCh38
NC_000001.10:g.160007265A= , CM000663.1:g.160007265A= GRCh37
NC_000001.9:g.158273889A= NCBI36
NG_016411.1:g.37697T=

Transcript Alleles

HGVS Amino-acid change
ENST00000509700.2:c.671+4359T=
ENST00000637644.1:c.487+4571T= ENSP00000490282.1:n.487+4571T=
ENST00000639408.1:c.587+3027T= ENSP00000491635.1:n.587+3027T=
ENST00000640914.1:c.224+3027T=
ENST00000644903.1:c.*3918T= MANE Select ENSP00000495557.1:n.*3918T=
ENST00000368089.3:c.*3918T= ENSP00000357068.3:n.*3918T=
NM_002241.4:c.*3918T= NP_002232.2:n.*3918T=
NM_002241.5:c.*3918T= MANE Select NP_002232.2:n.*3918T=