Canonical Allele Identifier: CA526593725

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1475178012
• gnomAD v2: 1-160007345-A-T
• MyVariant Identifiers: chr1:g.160007345A>T (hg19) ; chr1:g.160037555A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160037555A>T , CM000663.2:g.160037555A>T	GRCh38
NC_000001.10:g.160007345A>T , CM000663.1:g.160007345A>T	GRCh37
NC_000001.9:g.158273969A>T	NCBI36
NG_016411.1:g.37617T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000509700.2:c.671+4279T>A
ENST00000637644.1:c.487+4491T>A	ENSP00000490282.1:n.487+4491T>A
ENST00000639408.1:c.587+2947T>A	ENSP00000491635.1:n.587+2947T>A
ENST00000640914.1:c.224+2947T>A
ENST00000644903.1:c.*3838T>A MANE Select	ENSP00000495557.1:n.*3838T>A
ENST00000368089.3:c.*3838T>A	ENSP00000357068.3:n.*3838T>A
NM_002241.4:c.*3838T>A	NP_002232.2:n.*3838T>A
NM_002241.5:c.*3838T>A MANE Select	NP_002232.2:n.*3838T>A