Canonical Allele Identifier: CA15916133

Gene: KCNJ16

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.70094066C>T , CM000679.2:g.70094066C>T	GRCh38
NC_000017.10:g.68090207C>T , CM000679.1:g.68090207C>T	GRCh37
NC_000017.9:g.65601802C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392671.6:c.-299-6592C>T MANE Select	ENSP00000376439.1:n.-299-6592C>T
ENST00000283936.5:c.-380-6592C>T	ENSP00000283936.1:n.-380-6592C>T
ENST00000392671.5:c.-299-6592C>T	ENSP00000376439.1:n.-299-6592C>T
ENST00000588112.1:n.146-6592C>T
ENST00000589377.1:c.-94+18676C>T	ENSP00000465967.1:n.-94+18676C>T
ENST00000591891.5:c.-271-14235C>T	ENSP00000465646.1:n.-271-14235C>T
ENST00000615244.4:c.-508-6592C>T	ENSP00000479817.1:n.-508-6592C>T
NM_001270422.1:c.-508-6592C>T	NP_001257351.1:n.-508-6592C>T
NM_001291622.1:c.-357-6592C>T	NP_001278551.1:n.-357-6592C>T
NM_018658.2:c.-275-6592C>T	NP_061128.2:n.-275-6592C>T
NM_170741.2:c.-194-6592C>T	NP_733937.2:n.-194-6592C>T
XM_005257337.3:c.-86+18676C>T	XP_005257394.1:n.-86+18676C>T
XM_006721885.2:c.-491-6592C>T	XP_006721948.1:n.-491-6592C>T
XM_006721886.2:c.-363-6592C>T	XP_006721949.1:n.-363-6592C>T
XM_006721887.2:c.-356-6592C>T	XP_006721950.1:n.-356-6592C>T
XM_011524780.1:c.-545-6592C>T	XP_011523082.1:n.-545-6592C>T
XM_011524781.1:c.-427-6592C>T	XP_011523083.1:n.-427-6592C>T
XM_005257337.4:c.-86+18676C>T	XP_005257394.1:n.-86+18676C>T
XM_006721885.3:c.-491-6592C>T	XP_006721948.1:n.-491-6592C>T
XM_006721886.3:c.-363-6592C>T	XP_006721949.1:n.-363-6592C>T
XM_006721887.3:c.-356-6592C>T	XP_006721950.1:n.-356-6592C>T
XM_011524781.2:c.-427-6592C>T	XP_011523083.1:n.-427-6592C>T
XM_017024609.1:c.-594-6592C>T	XP_016880098.1:n.-594-6592C>T
XM_017024610.1:c.-329-6592C>T	XP_016880099.1:n.-329-6592C>T
NM_001270422.2:c.-508-6592C>T	NP_001257351.1:n.-508-6592C>T
NM_001291622.3:c.-462-6592C>T	NP_001278551.2:n.-462-6592C>T
NM_018658.4:c.-380-6592C>T	NP_061128.3:n.-380-6592C>T
NM_170741.4:c.-299-6592C>T MANE Select	NP_733937.3:n.-299-6592C>T