Canonical Allele Identifier: CA578701580
Gene: KCNH2 HGNC NCBI

Linked Data

dbSNP Id: rs1584846553

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948411_150948412insCCCCCCCCCCCCCCCCCCCCCCCCCC , CM000669.2:g.150948411_150948412insCCCCCCCCCCCCCCCCCCCCCCCCCC GRCh38
NC_000007.13:g.150645499_150645500insCCCCCCCCCCCCCCCCCCCCCCCCCC , CM000669.1:g.150645499_150645500insCCCCCCCCCCCCCCCCCCCCCCCCCC GRCh37
NC_000007.12:g.150276432_150276433insCCCCCCCCCCCCCCCCCCCCCCCCCC NCBI36
NG_008916.1:g.34519_34520insGGGGGGGGGGGGGGGGGGGGGGGGGG , LRG_288:g.34519_34520insGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

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