Canonical Allele Identifier: CA421597889

Gene: KCNJ10

Linked Data

• MyVariant Identifiers: chr1:g.160012251C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160042461C>A , CM000663.2:g.160042461C>A	GRCh38
NC_000001.10:g.160012251C>A , CM000663.1:g.160012251C>A	GRCh37
NC_000001.9:g.158278875C>A	NCBI36
NG_016411.1:g.32711G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.44G>T
ENST00000636689.1:n.95-3113G>T
ENST00000637644.1:c.72G>T	ENSP00000490282.1:p.Gly24=
ENST00000638728.1:c.72G>T	ENSP00000492619.1:p.Gly24=
ENST00000638868.1:c.72G>T	ENSP00000491250.1:p.Gly24=
ENST00000639408.1:c.72G>T	ENSP00000491635.1:p.Gly24=
ENST00000640017.1:c.42G>T	ENSP00000491337.1:p.Gly14=
ENST00000644903.1:c.72G>T MANE Select	ENSP00000495557.1:p.Gly24=
ENST00000368089.3:c.72G>T	ENSP00000357068.3:p.Gly24=
NM_002241.4:c.72G>T	NP_002232.2:p.Gly24=
NM_002241.5:c.72G>T MANE Select	NP_002232.2:p.Gly24=