Canonical Allele Identifier: CA2685602624

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150948424-C-CCA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948425_150948426insAC , CM000669.2:g.150948425_150948426insAC	GRCh38
NC_000007.13:g.150645513_150645514insAC , CM000669.1:g.150645513_150645514insAC	GRCh37
NC_000007.12:g.150276446_150276447insAC	NCBI36
NG_008916.1:g.34502_34503insTG , LRG_288:g.34502_34503insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3525+19_3525+20insTG
ENST00000262186.10:c.2692+19_2692+20insTG MANE Select	ENSP00000262186.5:n.2692+19_2692+20insTG
ENST00000330883.9:c.1672+19_1672+20insTG	ENSP00000328531.4:n.1672+19_1672+20insTG
ENST00000262186.9:c.2692+19_2692+20insTG	ENSP00000262186.5:n.2692+19_2692+20insTG
ENST00000330883.8:c.1672+19_1672+20insTG	ENSP00000328531.4:n.1672+19_1672+20insTG
NM_000238.3:c.2692+19_2692+20insTG , LRG_288t1:c.2692+19_2692+20insTG	NP_000229.1:n.2692+19_2692+20insTG
NM_172057.2:c.1672+19_1672+20insTG , LRG_288t3:c.1672+19_1672+20insTG	NP_742054.1:n.1672+19_1672+20insTG
XM_011516185.1:c.2392+19_2392+20insTG	XP_011514487.1:n.2392+19_2392+20insTG
XM_011516186.1:c.2692+19_2692+20insTG	XP_011514488.1:n.2692+19_2692+20insTG
XM_011516185.2:c.2392+19_2392+20insTG	XP_011514487.1:n.2392+19_2392+20insTG
XM_011516186.3:c.2692+19_2692+20insTG	XP_011514488.1:n.2692+19_2692+20insTG
XM_017012195.1:c.2542+19_2542+20insTG	XP_016867684.1:n.2542+19_2542+20insTG
XM_017012196.1:c.2515+19_2515+20insTG	XP_016867685.1:n.2515+19_2515+20insTG
NM_000238.4:c.2692+19_2692+20insTG MANE Select	NP_000229.1:n.2692+19_2692+20insTG
NM_172057.3:c.1672+19_1672+20insTG	NP_742054.1:n.1672+19_1672+20insTG