Canonical Allele Identifier: CA1008314868

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1648584806
• gnomAD v3: 1-160040944-C-CAAGGTG
• gnomAD v4: 1-160040944-C-CAAGGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160040946_160040947insGGTGAA , CM000663.2:g.160040946_160040947insGGTGAA	GRCh38
NC_000001.10:g.160010736_160010737insGGTGAA , CM000663.1:g.160010736_160010737insGGTGAA	GRCh37
NC_000001.9:g.158277360_158277361insGGTGAA	NCBI36
NG_016411.1:g.34227_34228insCACCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+889_671+890insCACCTT
ENST00000636689.1:n.95-1597_95-1596insCACCTT
ENST00000637644.1:c.487+1101_487+1102insCACCTT	ENSP00000490282.1:n.487+1101_487+1102insCACCTT
ENST00000638728.1:c.*448_*449insCACCTT	ENSP00000492619.1:n.*448_*449insCACCTT
ENST00000638840.1:c.920-344_920-343insCACCTT
ENST00000638868.1:c.*448_*449insCACCTT	ENSP00000491250.1:n.*448_*449insCACCTT
ENST00000639408.1:c.488-344_488-343insCACCTT	ENSP00000491635.1:n.488-344_488-343insCACCTT
ENST00000640017.1:c.670-344_670-343insCACCTT	ENSP00000491337.1:n.670-344_670-343insCACCTT
ENST00000640914.1:c.125-344_125-343insCACCTT
ENST00000644903.1:c.*448_*449insCACCTT MANE Select	ENSP00000495557.1:n.*448_*449insCACCTT
ENST00000368089.3:c.*448_*449insCACCTT	ENSP00000357068.3:n.*448_*449insCACCTT
ENST00000509700.1:n.463-344_463-343insCACCTT
NM_002241.4:c.*448_*449insCACCTT	NP_002232.2:n.*448_*449insCACCTT
NM_002241.5:c.*448_*449insCACCTT MANE Select	NP_002232.2:n.*448_*449insCACCTT