Canonical Allele Identifier: CA343221737

Gene: KCNJ10

Linked Data

• gnomAD v4: 1-160041406-A-T
• MyVariant Identifiers: chr1:g.160011196A>T (hg19) ; chr1:g.160041406A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041406A>T , CM000663.2:g.160041406A>T	GRCh38
NC_000001.10:g.160011196A>T , CM000663.1:g.160011196A>T	GRCh37
NC_000001.9:g.158277820A>T	NCBI36
NG_016411.1:g.33766T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+428T>A
ENST00000636689.1:n.95-2058T>A
ENST00000637644.1:c.487+640T>A	ENSP00000490282.1:n.487+640T>A
ENST00000638728.1:c.1127T>A	ENSP00000492619.1:p.Ile376Asn
ENST00000638840.1:c.849T>A
ENST00000638868.1:c.1127T>A	ENSP00000491250.1:p.Ile376Asn
ENST00000639408.1:c.487+640T>A	ENSP00000491635.1:n.487+640T>A
ENST00000640017.1:c.669+428T>A	ENSP00000491337.1:n.669+428T>A
ENST00000640914.1:c.124+428T>A
ENST00000644903.1:c.1127T>A MANE Select	ENSP00000495557.1:p.Ile376Asn
ENST00000368089.3:c.1127T>A	ENSP00000357068.3:p.Ile376Asn
ENST00000509700.1:n.462+428T>A
NM_002241.4:c.1127T>A	NP_002232.2:p.Ile376Asn
NM_002241.5:c.1127T>A MANE Select	NP_002232.2:p.Ile376Asn