Canonical Allele Identifier: CA473515715

Gene: KCNJ11

Linked Data

• MyVariant Identifiers: chr11:g.17409576A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388029A>G , CM000673.2:g.17388029A>G	GRCh38
NC_000011.9:g.17409576A>G , CM000673.1:g.17409576A>G	GRCh37
NC_000011.8:g.17366152A>G	NCBI36
NG_012446.1:g.5631T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000528992.2:c.-166T>C	ENSP00000436479.2:n.-166T>C
ENST00000682350.1:c.-16-183T>C	ENSP00000508090.1:n.-16-183T>C
ENST00000682764.1:c.-16-183T>C	ENSP00000506780.1:n.-16-183T>C
ENST00000339994.5:c.63T>C MANE Select	ENSP00000345708.4:p.Pro21=
ENST00000339994.4:c.63T>C	ENSP00000345708.4:p.Pro21=
ENST00000526912.1:c.-28T>C	ENSP00000432729.1:n.-28T>C
ENST00000528731.1:c.-16-183T>C	ENSP00000434755.1:n.-16-183T>C
ENST00000528992.1:c.80T>C
NM_000525.3:c.63T>C	NP_000516.3:p.Pro21=
NM_001166290.1:c.-16-183T>C	NP_001159762.1:n.-16-183T>C
XM_006718226.2:c.-16-183T>C	XP_006718289.1:n.-16-183T>C
XR_930867.1:n.221T>C
XM_006718226.3:c.-16-183T>C	XP_006718289.1:n.-16-183T>C
XM_017017680.1:c.-16-183T>C	XP_016873169.1:n.-16-183T>C
NM_001166290.2:c.-16-183T>C	NP_001159762.1:n.-16-183T>C
NM_001377296.1:c.-28T>C	NP_001364225.1:n.-28T>C
NM_001377297.1:c.-16-183T>C	NP_001364226.1:n.-16-183T>C
NM_000525.4:c.63T>C MANE Select	NP_000516.3:p.Pro21=