Canonical Allele Identifier: CA578701586
Gene: KCNH2 HGNC NCBI

Linked Data

dbSNP Id: rs1584846553

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948411_150948412insCCCCCCC , CM000669.2:g.150948411_150948412insCCCCCCC GRCh38
NC_000007.13:g.150645499_150645500insCCCCCCC , CM000669.1:g.150645499_150645500insCCCCCCC GRCh37
NC_000007.12:g.150276432_150276433insCCCCCCC NCBI36
NG_008916.1:g.34519_34520insGGGGGGG , LRG_288:g.34519_34520insGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.3525+36_3525+37insGGGGGGG
ENST00000262186.10:c.2692+36_2692+37insGGGGGGG MANE Select ENSP00000262186.5:n.2692+36_2692+37insGGGGGGG
ENST00000330883.9:c.1672+36_1672+37insGGGGGGG ENSP00000328531.4:n.1672+36_1672+37insGGGGGGG
ENST00000262186.9:c.2692+36_2692+37insGGGGGGG ENSP00000262186.5:n.2692+36_2692+37insGGGGGGG
ENST00000330883.8:c.1672+36_1672+37insGGGGGGG ENSP00000328531.4:n.1672+36_1672+37insGGGGGGG
NM_000238.3:c.2692+36_2692+37insGGGGGGG , LRG_288t1:c.2692+36_2692+37insGGGGGGG NP_000229.1:n.2692+36_2692+37insGGGGGGG
NM_172057.2:c.1672+36_1672+37insGGGGGGG , LRG_288t3:c.1672+36_1672+37insGGGGGGG NP_742054.1:n.1672+36_1672+37insGGGGGGG
XM_011516185.1:c.2392+36_2392+37insGGGGGGG XP_011514487.1:n.2392+36_2392+37insGGGGGGG
XM_011516186.1:c.2692+36_2692+37insGGGGGGG XP_011514488.1:n.2692+36_2692+37insGGGGGGG
XM_011516185.2:c.2392+36_2392+37insGGGGGGG XP_011514487.1:n.2392+36_2392+37insGGGGGGG
XM_011516186.3:c.2692+36_2692+37insGGGGGGG XP_011514488.1:n.2692+36_2692+37insGGGGGGG
XM_017012195.1:c.2542+36_2542+37insGGGGGGG XP_016867684.1:n.2542+36_2542+37insGGGGGGG
XM_017012196.1:c.2515+36_2515+37insGGGGGGG XP_016867685.1:n.2515+36_2515+37insGGGGGGG
NM_000238.4:c.2692+36_2692+37insGGGGGGG MANE Select NP_000229.1:n.2692+36_2692+37insGGGGGGG
NM_172057.3:c.1672+36_1672+37insGGGGGGG NP_742054.1:n.1672+36_1672+37insGGGGGGG