Canonical Allele Identifier: CA369853452
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150947815C>G , CM000669.2:g.150947815C>G GRCh38
NC_000007.13:g.150644903C>G , CM000669.1:g.150644903C>G GRCh37
NC_000007.12:g.150275836C>G NCBI36
NG_008916.1:g.35112G>C , LRG_288:g.35112G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.3589G>C
ENST00000262186.10:c.2756G>C MANE Select ENSP00000262186.5:p.Ser919Thr
ENST00000330883.9:c.1736G>C ENSP00000328531.4:p.Ser579Thr
ENST00000262186.9:c.2756G>C ENSP00000262186.5:p.Ser919Thr
ENST00000330883.8:c.1736G>C ENSP00000328531.4:p.Ser579Thr
NM_000238.3:c.2756G>C , LRG_288t1:c.2756G>C NP_000229.1:p.Ser919Thr
NM_172057.2:c.1736G>C , LRG_288t3:c.1736G>C NP_742054.1:p.Ser579Thr
XM_011516185.1:c.2456G>C XP_011514487.1:p.Ser819Thr
XM_011516186.1:c.2693-124G>C XP_011514488.1:n.2693-124G>C
XM_011516185.2:c.2456G>C XP_011514487.1:p.Ser819Thr
XM_011516186.3:c.2693-124G>C XP_011514488.1:n.2693-124G>C
XM_017012195.1:c.2606G>C XP_016867684.1:p.Ser869Thr
XM_017012196.1:c.2579G>C XP_016867685.1:p.Ser860Thr
NM_000238.4:c.2756G>C MANE Select NP_000229.1:p.Ser919Thr
NM_172057.3:c.1736G>C NP_742054.1:p.Ser579Thr