Canonical Allele Identifier: CA343230598

Gene: KCNJ10

Linked Data

• gnomAD v4: 1-160042463-C-G
• MyVariant Identifiers: chr1:g.160012253C>G (hg19) ; chr1:g.160042463C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160042463C>G , CM000663.2:g.160042463C>G	GRCh38
NC_000001.10:g.160012253C>G , CM000663.1:g.160012253C>G	GRCh37
NC_000001.9:g.158278877C>G	NCBI36
NG_016411.1:g.32709G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.42G>C
ENST00000636689.1:n.95-3115G>C
ENST00000637644.1:c.70G>C	ENSP00000490282.1:p.Gly24Arg
ENST00000638728.1:c.70G>C	ENSP00000492619.1:p.Gly24Arg
ENST00000638868.1:c.70G>C	ENSP00000491250.1:p.Gly24Arg
ENST00000639408.1:c.70G>C	ENSP00000491635.1:p.Gly24Arg
ENST00000640017.1:c.40G>C	ENSP00000491337.1:p.Gly14Arg
ENST00000644903.1:c.70G>C MANE Select	ENSP00000495557.1:p.Gly24Arg
ENST00000368089.3:c.70G>C	ENSP00000357068.3:p.Gly24Arg
NM_002241.4:c.70G>C	NP_002232.2:p.Gly24Arg
NM_002241.5:c.70G>C MANE Select	NP_002232.2:p.Gly24Arg