Canonical Allele Identifier: CA2685602548
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948416_150948417insTCCCCCCCCCCC , CM000669.2:g.150948416_150948417insTCCCCCCCCCCC GRCh38
NC_000007.13:g.150645504_150645505insTCCCCCCCCCCC , CM000669.1:g.150645504_150645505insTCCCCCCCCCCC GRCh37
NC_000007.12:g.150276437_150276438insTCCCCCCCCCCC NCBI36
NG_008916.1:g.34510_34511insGGGGGGGGGGGA , LRG_288:g.34510_34511insGGGGGGGGGGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.3525+27_3525+28insGGGGGGGGGGGA
ENST00000262186.10:c.2692+27_2692+28insGGGGGGGGGGGA MANE Select ENSP00000262186.5:n.2692+27_2692+28insGGGGGGGGGGGA
ENST00000330883.9:c.1672+27_1672+28insGGGGGGGGGGGA ENSP00000328531.4:n.1672+27_1672+28insGGGGGGGGGGGA
ENST00000262186.9:c.2692+27_2692+28insGGGGGGGGGGGA ENSP00000262186.5:n.2692+27_2692+28insGGGGGGGGGGGA
ENST00000330883.8:c.1672+27_1672+28insGGGGGGGGGGGA ENSP00000328531.4:n.1672+27_1672+28insGGGGGGGGGGGA
NM_000238.3:c.2692+27_2692+28insGGGGGGGGGGGA , LRG_288t1:c.2692+27_2692+28insGGGGGGGGGGGA NP_000229.1:n.2692+27_2692+28insGGGGGGGGGGGA
NM_172057.2:c.1672+27_1672+28insGGGGGGGGGGGA , LRG_288t3:c.1672+27_1672+28insGGGGGGGGGGGA NP_742054.1:n.1672+27_1672+28insGGGGGGGGGGGA
XM_011516185.1:c.2392+27_2392+28insGGGGGGGGGGGA XP_011514487.1:n.2392+27_2392+28insGGGGGGGGGGGA
XM_011516186.1:c.2692+27_2692+28insGGGGGGGGGGGA XP_011514488.1:n.2692+27_2692+28insGGGGGGGGGGGA
XM_011516185.2:c.2392+27_2392+28insGGGGGGGGGGGA XP_011514487.1:n.2392+27_2392+28insGGGGGGGGGGGA
XM_011516186.3:c.2692+27_2692+28insGGGGGGGGGGGA XP_011514488.1:n.2692+27_2692+28insGGGGGGGGGGGA
XM_017012195.1:c.2542+27_2542+28insGGGGGGGGGGGA XP_016867684.1:n.2542+27_2542+28insGGGGGGGGGGGA
XM_017012196.1:c.2515+27_2515+28insGGGGGGGGGGGA XP_016867685.1:n.2515+27_2515+28insGGGGGGGGGGGA
NM_000238.4:c.2692+27_2692+28insGGGGGGGGGGGA MANE Select NP_000229.1:n.2692+27_2692+28insGGGGGGGGGGGA
NM_172057.3:c.1672+27_1672+28insGGGGGGGGGGGA NP_742054.1:n.1672+27_1672+28insGGGGGGGGGGGA