Canonical Allele Identifier: CA578701699
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948425_150948426insCCCCCCCCC , CM000669.2:g.150948425_150948426insCCCCCCCCC GRCh38
NC_000007.13:g.150645513_150645514insCCCCCCCCC , CM000669.1:g.150645513_150645514insCCCCCCCCC GRCh37
NC_000007.12:g.150276446_150276447insCCCCCCCCC NCBI36
NG_008916.1:g.34503_34504insGGGGGGGGG , LRG_288:g.34503_34504insGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.3525+20_3525+21insGGGGGGGGG
ENST00000262186.10:c.2692+20_2692+21insGGGGGGGGG MANE Select ENSP00000262186.5:n.2692+20_2692+21insGGGGGGGGG
ENST00000330883.9:c.1672+20_1672+21insGGGGGGGGG ENSP00000328531.4:n.1672+20_1672+21insGGGGGGGGG
ENST00000262186.9:c.2692+20_2692+21insGGGGGGGGG ENSP00000262186.5:n.2692+20_2692+21insGGGGGGGGG
ENST00000330883.8:c.1672+20_1672+21insGGGGGGGGG ENSP00000328531.4:n.1672+20_1672+21insGGGGGGGGG
NM_000238.3:c.2692+20_2692+21insGGGGGGGGG , LRG_288t1:c.2692+20_2692+21insGGGGGGGGG NP_000229.1:n.2692+20_2692+21insGGGGGGGGG
NM_172057.2:c.1672+20_1672+21insGGGGGGGGG , LRG_288t3:c.1672+20_1672+21insGGGGGGGGG NP_742054.1:n.1672+20_1672+21insGGGGGGGGG
XM_011516185.1:c.2392+20_2392+21insGGGGGGGGG XP_011514487.1:n.2392+20_2392+21insGGGGGGGGG
XM_011516186.1:c.2692+20_2692+21insGGGGGGGGG XP_011514488.1:n.2692+20_2692+21insGGGGGGGGG
XM_011516185.2:c.2392+20_2392+21insGGGGGGGGG XP_011514487.1:n.2392+20_2392+21insGGGGGGGGG
XM_011516186.3:c.2692+20_2692+21insGGGGGGGGG XP_011514488.1:n.2692+20_2692+21insGGGGGGGGG
XM_017012195.1:c.2542+20_2542+21insGGGGGGGGG XP_016867684.1:n.2542+20_2542+21insGGGGGGGGG
XM_017012196.1:c.2515+20_2515+21insGGGGGGGGG XP_016867685.1:n.2515+20_2515+21insGGGGGGGGG
NM_000238.4:c.2692+20_2692+21insGGGGGGGGG MANE Select NP_000229.1:n.2692+20_2692+21insGGGGGGGGG
NM_172057.3:c.1672+20_1672+21insGGGGGGGGG NP_742054.1:n.1672+20_1672+21insGGGGGGGGG