Canonical Allele Identifier: CA2685602676

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150948429-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948429_150948430insAG , CM000669.2:g.150948429_150948430insAG	GRCh38
NC_000007.13:g.150645517_150645518insAG , CM000669.1:g.150645517_150645518insAG	GRCh37
NC_000007.12:g.150276450_150276451insAG	NCBI36
NG_008916.1:g.34497_34498insCT , LRG_288:g.34497_34498insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3525+14_3525+15insCT
ENST00000262186.10:c.2692+14_2692+15insCT MANE Select	ENSP00000262186.5:n.2692+14_2692+15insCT
ENST00000330883.9:c.1672+14_1672+15insCT	ENSP00000328531.4:n.1672+14_1672+15insCT
ENST00000262186.9:c.2692+14_2692+15insCT	ENSP00000262186.5:n.2692+14_2692+15insCT
ENST00000330883.8:c.1672+14_1672+15insCT	ENSP00000328531.4:n.1672+14_1672+15insCT
NM_000238.3:c.2692+14_2692+15insCT , LRG_288t1:c.2692+14_2692+15insCT	NP_000229.1:n.2692+14_2692+15insCT
NM_172057.2:c.1672+14_1672+15insCT , LRG_288t3:c.1672+14_1672+15insCT	NP_742054.1:n.1672+14_1672+15insCT
XM_011516185.1:c.2392+14_2392+15insCT	XP_011514487.1:n.2392+14_2392+15insCT
XM_011516186.1:c.2692+14_2692+15insCT	XP_011514488.1:n.2692+14_2692+15insCT
XM_011516185.2:c.2392+14_2392+15insCT	XP_011514487.1:n.2392+14_2392+15insCT
XM_011516186.3:c.2692+14_2692+15insCT	XP_011514488.1:n.2692+14_2692+15insCT
XM_017012195.1:c.2542+14_2542+15insCT	XP_016867684.1:n.2542+14_2542+15insCT
XM_017012196.1:c.2515+14_2515+15insCT	XP_016867685.1:n.2515+14_2515+15insCT
NM_000238.4:c.2692+14_2692+15insCT MANE Select	NP_000229.1:n.2692+14_2692+15insCT
NM_172057.3:c.1672+14_1672+15insCT	NP_742054.1:n.1672+14_1672+15insCT