Canonical Allele Identifier: CA477703812

Gene: KCNJ5

Linked Data

• COSMIC: COSM3445206
• MyVariant Identifiers: chr11:g.128781825C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128911930C>T , CM000673.2:g.128911930C>T	GRCh38
NC_000011.9:g.128781825C>T , CM000673.1:g.128781825C>T	GRCh37
NC_000011.8:g.128287035C>T	NCBI36
NG_023406.2:g.25513C>T , LRG_333:g.25513C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000529694.6:c.657C>T MANE Select	ENSP00000433295.1:p.Phe219=
ENST00000338350.4:c.657C>T	ENSP00000339960.4:p.Phe219=
ENST00000529694.5:c.657C>T	ENSP00000433295.1:p.Phe219=
ENST00000533599.1:c.657C>T	ENSP00000434266.1:p.Phe219=
NM_000890.3:c.657C>T , LRG_333t1:c.657C>T	NP_000881.3:p.Phe219=
XM_011542809.1:c.657C>T	XP_011541111.1:p.Phe219=
XM_011542810.1:c.657C>T	XP_011541112.1:p.Phe219=
NM_000890.4:c.657C>T	NP_000881.3:p.Phe219=
NM_001354169.1:c.657C>T	NP_001341098.1:p.Phe219=
XM_011542809.2:c.657C>T	XP_011541111.1:p.Phe219=
XM_011542810.3:c.657C>T	XP_011541112.1:p.Phe219=
NM_000890.5:c.657C>T MANE Select	NP_000881.3:p.Phe219=
NM_001354169.2:c.657C>T	NP_001341098.1:p.Phe219=