Canonical Allele Identifier: CA2648631537

Gene: KCNJ10

Linked Data

• gnomAD v4: 1-160041141-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041141C>G , CM000663.2:g.160041141C>G	GRCh38
NC_000001.10:g.160010931C>G , CM000663.1:g.160010931C>G	GRCh37
NC_000001.9:g.158277555C>G	NCBI36
NG_016411.1:g.34031G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+693G>C
ENST00000636689.1:n.95-1793G>C
ENST00000637644.1:c.487+905G>C	ENSP00000490282.1:n.487+905G>C
ENST00000638728.1:c.*252G>C	ENSP00000492619.1:n.*252G>C
ENST00000638840.1:c.919+195G>C
ENST00000638868.1:c.*252G>C	ENSP00000491250.1:n.*252G>C
ENST00000639408.1:c.488-540G>C	ENSP00000491635.1:n.488-540G>C
ENST00000640017.1:c.670-540G>C	ENSP00000491337.1:n.670-540G>C
ENST00000640914.1:c.125-540G>C
ENST00000644903.1:c.*252G>C MANE Select	ENSP00000495557.1:n.*252G>C
ENST00000368089.3:c.*252G>C	ENSP00000357068.3:n.*252G>C
ENST00000509700.1:n.463-540G>C
NM_002241.4:c.*252G>C	NP_002232.2:n.*252G>C
NM_002241.5:c.*252G>C MANE Select	NP_002232.2:n.*252G>C