Canonical Allele Identifier: CA14477588

Gene: KCNJ16

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.70112276T>C , CM000679.2:g.70112276T>C	GRCh38
NC_000017.10:g.68108417T>C , CM000679.1:g.68108417T>C	GRCh37
NC_000017.9:g.65620012T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392671.6:c.-191+11510T>C MANE Select	ENSP00000376439.1:n.-191+11510T>C
ENST00000283936.5:c.-191+3895T>C	ENSP00000283936.1:n.-191+3895T>C
ENST00000392670.5:c.-191+3895T>C	ENSP00000376438.1:n.-191+3895T>C
ENST00000392671.5:c.-191+11510T>C	ENSP00000376439.1:n.-191+11510T>C
ENST00000585558.5:c.-86+3895T>C	ENSP00000465295.1:n.-86+3895T>C
ENST00000586462.1:c.24+15350T>C	ENSP00000467568.1:n.24+15350T>C
ENST00000587698.5:c.-319+7201T>C	ENSP00000466132.1:n.-319+7201T>C
ENST00000587892.1:c.-319+3895T>C	ENSP00000465163.1:n.-319+3895T>C
ENST00000589377.1:c.-93-19719T>C	ENSP00000465967.1:n.-93-19719T>C
ENST00000591891.5:c.-191+3895T>C	ENSP00000465646.1:n.-191+3895T>C
ENST00000615244.4:c.-319+3895T>C	ENSP00000479817.1:n.-319+3895T>C
NM_001270422.1:c.-319+3895T>C	NP_001257351.1:n.-319+3895T>C
NM_001291622.1:c.-86+1834T>C	NP_001278551.1:n.-86+1834T>C
NM_001291623.1:c.-86+7201T>C	NP_001278552.1:n.-86+7201T>C
NM_001291624.1:c.-319+7201T>C	NP_001278553.1:n.-319+7201T>C
NM_001291625.1:c.-319+3895T>C	NP_001278554.1:n.-319+3895T>C
NM_018658.2:c.-86+3895T>C	NP_061128.2:n.-86+3895T>C
NM_170741.2:c.-86+11510T>C	NP_733937.2:n.-86+11510T>C
NM_170742.2:c.-86+3895T>C	NP_733938.2:n.-86+3895T>C
XM_005257337.3:c.-85-18603T>C	XP_005257394.1:n.-85-18603T>C
XM_006721885.2:c.-86+3895T>C	XP_006721948.1:n.-86+3895T>C
XM_006721886.2:c.-86+3895T>C	XP_006721949.1:n.-86+3895T>C
XM_006721887.2:c.-86+3895T>C	XP_006721950.1:n.-86+3895T>C
XM_011524780.1:c.-140+3895T>C	XP_011523082.1:n.-140+3895T>C
XM_011524781.1:c.-319+11510T>C	XP_011523083.1:n.-319+11510T>C
XM_005257337.4:c.-85-18603T>C	XP_005257394.1:n.-85-18603T>C
XM_006721885.3:c.-86+3895T>C	XP_006721948.1:n.-86+3895T>C
XM_006721886.3:c.-86+3895T>C	XP_006721949.1:n.-86+3895T>C
XM_006721887.3:c.-86+3895T>C	XP_006721950.1:n.-86+3895T>C
XM_011524781.2:c.-319+11510T>C	XP_011523083.1:n.-319+11510T>C
XM_017024609.1:c.-86+3895T>C	XP_016880098.1:n.-86+3895T>C
XM_017024610.1:c.-140+3895T>C	XP_016880099.1:n.-140+3895T>C
NM_001270422.2:c.-319+3895T>C	NP_001257351.1:n.-319+3895T>C
NM_001291622.3:c.-191+1834T>C	NP_001278551.2:n.-191+1834T>C
NM_001291623.2:c.-191+7201T>C	NP_001278552.2:n.-191+7201T>C
NM_018658.4:c.-191+3895T>C	NP_061128.3:n.-191+3895T>C
NM_170741.4:c.-191+11510T>C MANE Select	NP_733937.3:n.-191+11510T>C
NM_170742.3:c.-191+3895T>C	NP_733938.3:n.-191+3895T>C