Canonical Allele Identifier: CA379770546

Gene: KCNJ11

Linked Data

• ClinVar Variation Id: 2179313
• ClinVar RCV Id: RCV002591887
• gnomAD v4: 11-17387281-C-T
• MyVariant Identifiers: chr11:g.17408828C>T (hg19) ; chr11:g.17387281C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387281C>T , CM000673.2:g.17387281C>T	GRCh38
NC_000011.9:g.17408828C>T , CM000673.1:g.17408828C>T	GRCh37
NC_000011.8:g.17365404C>T	NCBI36
NG_012446.1:g.6379G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682350.1:c.550G>A	ENSP00000508090.1:p.Ala184Thr
ENST00000682764.1:c.550G>A	ENSP00000506780.1:p.Ala184Thr
ENST00000339994.5:c.811G>A MANE Select	ENSP00000345708.4:p.Ala271Thr
ENST00000339994.4:c.811G>A	ENSP00000345708.4:p.Ala271Thr
ENST00000528731.1:c.550G>A	ENSP00000434755.1:p.Ala184Thr
NM_000525.3:c.811G>A	NP_000516.3:p.Ala271Thr
NM_001166290.1:c.550G>A	NP_001159762.1:p.Ala184Thr
XM_006718226.2:c.550G>A	XP_006718289.1:p.Ala184Thr
XR_930867.1:n.969G>A
XM_006718226.3:c.550G>A	XP_006718289.1:p.Ala184Thr
XM_017017680.1:c.550G>A	XP_016873169.1:p.Ala184Thr
NM_001166290.2:c.550G>A	NP_001159762.1:p.Ala184Thr
NM_001377296.1:c.550G>A	NP_001364225.1:p.Ala184Thr
NM_001377297.1:c.550G>A	NP_001364226.1:p.Ala184Thr
NM_000525.4:c.811G>A MANE Select	NP_000516.3:p.Ala271Thr