Canonical Allele Identifier: CA890088210

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1444127602
• gnomAD v3: 1-160037541-CT-C
• gnomAD v4: 1-160037541-CT-C
• MyVariant Identifiers: chr1:g.160007332del (hg19) ; chr1:g.160037542del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160037549del , CM000663.2:g.160037549del	GRCh38
NC_000001.10:g.160007339del , CM000663.1:g.160007339del	GRCh37
NC_000001.9:g.158273963del	NCBI36
NG_016411.1:g.37630del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+4292del
ENST00000637644.1:c.487+4504del	ENSP00000490282.1:n.487+4504del
ENST00000639408.1:c.587+2960del	ENSP00000491635.1:n.587+2960del
ENST00000640914.1:c.224+2960del
ENST00000644903.1:c.*3851del MANE Select	ENSP00000495557.1:n.*3851del
ENST00000368089.3:c.*3851del	ENSP00000357068.3:n.*3851del
NM_002241.4:c.*3851del	NP_002232.2:n.*3851del
NM_002241.5:c.*3851del MANE Select	NP_002232.2:n.*3851del