Canonical Allele Identifier: CA383235763

Gene: KCNJ5

Linked Data

• MyVariant Identifiers: chr11:g.128786417T>G (hg19) ; chr11:g.128916522T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916522T>G , CM000673.2:g.128916522T>G	GRCh38
NC_000011.9:g.128786417T>G , CM000673.1:g.128786417T>G	GRCh37
NC_000011.8:g.128291627T>G	NCBI36
NG_023406.2:g.30105T>G , LRG_333:g.30105T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529694.6:c.1051T>G MANE Select	ENSP00000433295.1:p.Phe351Val
ENST00000338350.4:c.1051T>G	ENSP00000339960.4:p.Phe351Val
ENST00000529694.5:c.1051T>G	ENSP00000433295.1:p.Phe351Val
ENST00000533599.1:c.1051T>G	ENSP00000434266.1:p.Phe351Val
NM_000890.3:c.1051T>G , LRG_333t1:c.1051T>G	NP_000881.3:p.Phe351Val
XM_011542809.1:c.1051T>G	XP_011541111.1:p.Phe351Val
XM_011542810.1:c.1051T>G	XP_011541112.1:p.Phe351Val
NM_000890.4:c.1051T>G	NP_000881.3:p.Phe351Val
NM_001354169.1:c.1051T>G	NP_001341098.1:p.Phe351Val
XM_011542809.2:c.1051T>G	XP_011541111.1:p.Phe351Val
XM_011542810.3:c.1051T>G	XP_011541112.1:p.Phe351Val
NM_000890.5:c.1051T>G MANE Select	NP_000881.3:p.Phe351Val
NM_001354169.2:c.1051T>G	NP_001341098.1:p.Phe351Val