Canonical Allele Identifier: CA379769270

Gene: KCNJ11

Linked Data

• MyVariant Identifiers: chr11:g.17408549C>G (hg19) ; chr11:g.17387002C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387002C>G , CM000673.2:g.17387002C>G	GRCh38
NC_000011.9:g.17408549C>G , CM000673.1:g.17408549C>G	GRCh37
NC_000011.8:g.17365125C>G	NCBI36
NG_012446.1:g.6658G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682350.1:c.829G>C	ENSP00000508090.1:p.Ala277Pro
ENST00000682764.1:c.829G>C	ENSP00000506780.1:p.Ala277Pro
ENST00000339994.5:c.1090G>C MANE Select	ENSP00000345708.4:p.Ala364Pro
ENST00000339994.4:c.1090G>C	ENSP00000345708.4:p.Ala364Pro
ENST00000528731.1:c.829G>C	ENSP00000434755.1:p.Ala277Pro
NM_000525.3:c.1090G>C	NP_000516.3:p.Ala364Pro
NM_001166290.1:c.829G>C	NP_001159762.1:p.Ala277Pro
XM_006718226.2:c.829G>C	XP_006718289.1:p.Ala277Pro
XR_930867.1:n.1248G>C
XM_006718226.3:c.829G>C	XP_006718289.1:p.Ala277Pro
XM_017017680.1:c.829G>C	XP_016873169.1:p.Ala277Pro
NM_001166290.2:c.829G>C	NP_001159762.1:p.Ala277Pro
NM_001377296.1:c.829G>C	NP_001364225.1:p.Ala277Pro
NM_001377297.1:c.829G>C	NP_001364226.1:p.Ala277Pro
NM_000525.4:c.1090G>C MANE Select	NP_000516.3:p.Ala364Pro