Canonical Allele Identifier: CA369853607
Gene: KCNH2 HGNC NCBI

Linked Data

dbSNP Id: rs758917587

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948445C>A , CM000669.2:g.150948445C>A GRCh38
NC_000007.13:g.150645533C>A , CM000669.1:g.150645533C>A GRCh37
NC_000007.12:g.150276466C>A NCBI36
NG_008916.1:g.34482G>T , LRG_288:g.34482G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.3524G>T
ENST00000262186.10:c.2691G>T MANE Select ENSP00000262186.5:p.Lys897Asn
ENST00000330883.9:c.1671G>T ENSP00000328531.4:p.Lys557Asn
ENST00000262186.9:c.2691G>T ENSP00000262186.5:p.Lys897Asn
ENST00000330883.8:c.1671G>T ENSP00000328531.4:p.Lys557Asn
NM_000238.3:c.2691G>T , LRG_288t1:c.2691G>T NP_000229.1:p.Lys897Asn
NM_172057.2:c.1671G>T , LRG_288t3:c.1671G>T NP_742054.1:p.Lys557Asn
XM_011516185.1:c.2391G>T XP_011514487.1:p.Lys797Asn
XM_011516186.1:c.2691G>T XP_011514488.1:p.Lys897Asn
XM_011516185.2:c.2391G>T XP_011514487.1:p.Lys797Asn
XM_011516186.3:c.2691G>T XP_011514488.1:p.Lys897Asn
XM_017012195.1:c.2541G>T XP_016867684.1:p.Lys847Asn
XM_017012196.1:c.2514G>T XP_016867685.1:p.Lys838Asn
NM_000238.4:c.2691G>T MANE Select NP_000229.1:p.Lys897Asn
NM_172057.3:c.1671G>T NP_742054.1:p.Lys557Asn