Canonical Allele Identifier: CA2685602591
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948421_150948422insCAACAACCCCAC , CM000669.2:g.150948421_150948422insCAACAACCCCAC GRCh38
NC_000007.13:g.150645509_150645510insCAACAACCCCAC , CM000669.1:g.150645509_150645510insCAACAACCCCAC GRCh37
NC_000007.12:g.150276442_150276443insCAACAACCCCAC NCBI36
NG_008916.1:g.34506_34507insTGGGGTTGTTGG , LRG_288:g.34506_34507insTGGGGTTGTTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.3525+23_3525+24insTGGGGTTGTTGG
ENST00000262186.10:c.2692+23_2692+24insTGGGGTTGTTGG MANE Select ENSP00000262186.5:n.2692+23_2692+24insTGGGGTTGTTGG
ENST00000330883.9:c.1672+23_1672+24insTGGGGTTGTTGG ENSP00000328531.4:n.1672+23_1672+24insTGGGGTTGTTGG
ENST00000262186.9:c.2692+23_2692+24insTGGGGTTGTTGG ENSP00000262186.5:n.2692+23_2692+24insTGGGGTTGTTGG
ENST00000330883.8:c.1672+23_1672+24insTGGGGTTGTTGG ENSP00000328531.4:n.1672+23_1672+24insTGGGGTTGTTGG
NM_000238.3:c.2692+23_2692+24insTGGGGTTGTTGG , LRG_288t1:c.2692+23_2692+24insTGGGGTTGTTGG NP_000229.1:n.2692+23_2692+24insTGGGGTTGTTGG
NM_172057.2:c.1672+23_1672+24insTGGGGTTGTTGG , LRG_288t3:c.1672+23_1672+24insTGGGGTTGTTGG NP_742054.1:n.1672+23_1672+24insTGGGGTTGTTGG
XM_011516185.1:c.2392+23_2392+24insTGGGGTTGTTGG XP_011514487.1:n.2392+23_2392+24insTGGGGTTGTTGG
XM_011516186.1:c.2692+23_2692+24insTGGGGTTGTTGG XP_011514488.1:n.2692+23_2692+24insTGGGGTTGTTGG
XM_011516185.2:c.2392+23_2392+24insTGGGGTTGTTGG XP_011514487.1:n.2392+23_2392+24insTGGGGTTGTTGG
XM_011516186.3:c.2692+23_2692+24insTGGGGTTGTTGG XP_011514488.1:n.2692+23_2692+24insTGGGGTTGTTGG
XM_017012195.1:c.2542+23_2542+24insTGGGGTTGTTGG XP_016867684.1:n.2542+23_2542+24insTGGGGTTGTTGG
XM_017012196.1:c.2515+23_2515+24insTGGGGTTGTTGG XP_016867685.1:n.2515+23_2515+24insTGGGGTTGTTGG
NM_000238.4:c.2692+23_2692+24insTGGGGTTGTTGG MANE Select NP_000229.1:n.2692+23_2692+24insTGGGGTTGTTGG
NM_172057.3:c.1672+23_1672+24insTGGGGTTGTTGG NP_742054.1:n.1672+23_1672+24insTGGGGTTGTTGG