Canonical Allele Identifier: CA2685602639

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150948425-C-CCCCCCCCCCCCCCCCCCCCCCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948425_150948426insCCCCCCCCCCCCCCCCCCCCCTT , CM000669.2:g.150948425_150948426insCCCCCCCCCCCCCCCCCCCCCTT	GRCh38
NC_000007.13:g.150645513_150645514insCCCCCCCCCCCCCCCCCCCCCTT , CM000669.1:g.150645513_150645514insCCCCCCCCCCCCCCCCCCCCCTT	GRCh37
NC_000007.12:g.150276446_150276447insCCCCCCCCCCCCCCCCCCCCCTT	NCBI36
NG_008916.1:g.34501_34502insAAGGGGGGGGGGGGGGGGGGGGG , LRG_288:g.34501_34502insAAGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3525+18_3525+19insAAGGGGGGGGGGGGGGGGGGGGG
ENST00000262186.10:c.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000262186.5:n.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG...
ENST00000330883.9:c.1672+18_1672+19insAAGGGGGGGGGGGGGGGGGGGGG	ENSP00000328531.4:n.1672+18_1672+19insAAGGGGGGGGGGGGGGGGGGGGG...
ENST00000262186.9:c.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG	ENSP00000262186.5:n.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG...
ENST00000330883.8:c.1672+18_1672+19insAAGGGGGGGGGGGGGGGGGGGGG	ENSP00000328531.4:n.1672+18_1672+19insAAGGGGGGGGGGGGGGGGGGGGG...
NM_000238.3:c.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG , LRG_288t1:c.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG	NP_000229.1:n.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG
NM_172057.2:c.1672+18_1672+19insAAGGGGGGGGGGGGGGGGGGGGG , LRG_288t3:c.1672+18_1672+19insAAGGGGGGGGGGGGGGGGGGGGG	NP_742054.1:n.1672+18_1672+19insAAGGGGGGGGGGGGGGGGGGGGG
XM_011516185.1:c.2392+18_2392+19insAAGGGGGGGGGGGGGGGGGGGGG	XP_011514487.1:n.2392+18_2392+19insAAGGGGGGGGGGGGGGGGGGGGG
XM_011516186.1:c.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG	XP_011514488.1:n.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG
XM_011516185.2:c.2392+18_2392+19insAAGGGGGGGGGGGGGGGGGGGGG	XP_011514487.1:n.2392+18_2392+19insAAGGGGGGGGGGGGGGGGGGGGG
XM_011516186.3:c.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG	XP_011514488.1:n.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG
XM_017012195.1:c.2542+18_2542+19insAAGGGGGGGGGGGGGGGGGGGGG	XP_016867684.1:n.2542+18_2542+19insAAGGGGGGGGGGGGGGGGGGGGG
XM_017012196.1:c.2515+18_2515+19insAAGGGGGGGGGGGGGGGGGGGGG	XP_016867685.1:n.2515+18_2515+19insAAGGGGGGGGGGGGGGGGGGGGG
NM_000238.4:c.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG MANE Select	NP_000229.1:n.2692+18_2692+19insAAGGGGGGGGGGGGGGGGGGGGG
NM_172057.3:c.1672+18_1672+19insAAGGGGGGGGGGGGGGGGGGGGG	NP_742054.1:n.1672+18_1672+19insAAGGGGGGGGGGGGGGGGGGGGG