Canonical Allele Identifier: CA477703367

Gene: KCNJ5

Linked Data

• COSMIC: COSM1665524
• MyVariant Identifiers: chr11:g.128781242del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128911348del , CM000673.2:g.128911348del	GRCh38
NC_000011.9:g.128781243del , CM000673.1:g.128781243del	GRCh37
NC_000011.8:g.128286453del	NCBI36
NG_023406.2:g.24931del , LRG_333:g.24931del

Transcript Alleles

HGVS	Amino-acid change
ENST00000529694.6:c.75del MANE Select	ENSP00000433295.1:p.Pro26GlnfsTer?
ENST00000338350.4:c.75del	ENSP00000339960.4:p.Pro26GlnfsTer?
ENST00000529694.5:c.75del	ENSP00000433295.1:p.Pro26GlnfsTer?
ENST00000533599.1:c.75del	ENSP00000434266.1:p.Pro26GlnfsTer?
NM_000890.3:c.75del , LRG_333t1:c.75del	NP_000881.3:p.Pro26GlnfsTer?
XM_011542809.1:c.75del	XP_011541111.1:p.Pro26GlnfsTer?
XM_011542810.1:c.75del	XP_011541112.1:p.Pro26GlnfsTer?
NM_000890.4:c.75del	NP_000881.3:p.Pro26GlnfsTer?
NM_001354169.1:c.75del	NP_001341098.1:p.Pro26GlnfsTer?
XM_011542809.2:c.75del	XP_011541111.1:p.Pro26GlnfsTer?
XM_011542810.3:c.75del	XP_011541112.1:p.Pro26GlnfsTer?
NM_000890.5:c.75del MANE Select	NP_000881.3:p.Pro26GlnfsTer?
NM_001354169.2:c.75del	NP_001341098.1:p.Pro26GlnfsTer?