Canonical Allele Identifier: CA2685602584
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948421_150948422insAAAAACC , CM000669.2:g.150948421_150948422insAAAAACC GRCh38
NC_000007.13:g.150645509_150645510insAAAAACC , CM000669.1:g.150645509_150645510insAAAAACC GRCh37
NC_000007.12:g.150276442_150276443insAAAAACC NCBI36
NG_008916.1:g.34507_34508insTTTTTGG , LRG_288:g.34507_34508insTTTTTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.3525+24_3525+25insTTTTTGG
ENST00000262186.10:c.2692+24_2692+25insTTTTTGG MANE Select ENSP00000262186.5:n.2692+24_2692+25insTTTTTGG
ENST00000330883.9:c.1672+24_1672+25insTTTTTGG ENSP00000328531.4:n.1672+24_1672+25insTTTTTGG
ENST00000262186.9:c.2692+24_2692+25insTTTTTGG ENSP00000262186.5:n.2692+24_2692+25insTTTTTGG
ENST00000330883.8:c.1672+24_1672+25insTTTTTGG ENSP00000328531.4:n.1672+24_1672+25insTTTTTGG
NM_000238.3:c.2692+24_2692+25insTTTTTGG , LRG_288t1:c.2692+24_2692+25insTTTTTGG NP_000229.1:n.2692+24_2692+25insTTTTTGG
NM_172057.2:c.1672+24_1672+25insTTTTTGG , LRG_288t3:c.1672+24_1672+25insTTTTTGG NP_742054.1:n.1672+24_1672+25insTTTTTGG
XM_011516185.1:c.2392+24_2392+25insTTTTTGG XP_011514487.1:n.2392+24_2392+25insTTTTTGG
XM_011516186.1:c.2692+24_2692+25insTTTTTGG XP_011514488.1:n.2692+24_2692+25insTTTTTGG
XM_011516185.2:c.2392+24_2392+25insTTTTTGG XP_011514487.1:n.2392+24_2392+25insTTTTTGG
XM_011516186.3:c.2692+24_2692+25insTTTTTGG XP_011514488.1:n.2692+24_2692+25insTTTTTGG
XM_017012195.1:c.2542+24_2542+25insTTTTTGG XP_016867684.1:n.2542+24_2542+25insTTTTTGG
XM_017012196.1:c.2515+24_2515+25insTTTTTGG XP_016867685.1:n.2515+24_2515+25insTTTTTGG
NM_000238.4:c.2692+24_2692+25insTTTTTGG MANE Select NP_000229.1:n.2692+24_2692+25insTTTTTGG
NM_172057.3:c.1672+24_1672+25insTTTTTGG NP_742054.1:n.1672+24_1672+25insTTTTTGG