Canonical Allele Identifier: CA1752431058
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948395A= , CM000669.2:g.150948395A= GRCh38
NC_000007.13:g.150645483A= , CM000669.1:g.150645483A= GRCh37
NC_000007.12:g.150276416A= NCBI36
NG_008916.1:g.34532T= , LRG_288:g.34532T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.3525+49T=
ENST00000262186.10:c.2692+49T= MANE Select ENSP00000262186.5:n.2692+49T=
ENST00000330883.9:c.1672+49T= ENSP00000328531.4:n.1672+49T=
ENST00000262186.9:c.2692+49T= ENSP00000262186.5:n.2692+49T=
ENST00000330883.8:c.1672+49T= ENSP00000328531.4:n.1672+49T=
NM_000238.3:c.2692+49T= , LRG_288t1:c.2692+49T= NP_000229.1:n.2692+49T=
NM_172057.2:c.1672+49T= , LRG_288t3:c.1672+49T= NP_742054.1:n.1672+49T=
XM_011516185.1:c.2392+49T= XP_011514487.1:n.2392+49T=
XM_011516186.1:c.2692+49T= XP_011514488.1:n.2692+49T=
XM_011516185.2:c.2392+49T= XP_011514487.1:n.2392+49T=
XM_011516186.3:c.2692+49T= XP_011514488.1:n.2692+49T=
XM_017012195.1:c.2542+49T= XP_016867684.1:n.2542+49T=
XM_017012196.1:c.2515+49T= XP_016867685.1:n.2515+49T=
NM_000238.4:c.2692+49T= MANE Select NP_000229.1:n.2692+49T=
NM_172057.3:c.1672+49T= NP_742054.1:n.1672+49T=