Canonical Allele Identifier: CA1752409376
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951481T= , CM000669.2:g.150951481T= GRCh38
NC_000007.13:g.150648569T= , CM000669.1:g.150648569T= GRCh37
NC_000007.12:g.150279502T= NCBI36
NG_008916.1:g.31446A= , LRG_288:g.31446A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1210A=
ENST00000683359.1:n.36A=
ENST00000684241.1:n.2745A=
ENST00000262186.10:c.1912A= MANE Select ENSP00000262186.5:p.Lys638=
ENST00000330883.9:c.892A= ENSP00000328531.4:p.Lys298=
ENST00000262186.9:c.1912A= ENSP00000262186.5:p.Lys638=
ENST00000330883.8:c.892A= ENSP00000328531.4:p.Lys298=
ENST00000430723.4:c.1564A= ENSP00000387657.4:p.Lys522=
ENST00000461280.1:n.1199A=
ENST00000473610.5:n.1217A=
ENST00000532957.5:n.2135A=
NM_000238.3:c.1912A= , LRG_288t1:c.1912A= NP_000229.1:p.Lys638=
NM_001204798.1:c.892A= NP_001191727.1:p.Lys298=
NM_172056.2:c.1912A= , LRG_288t2:c.1912A= NP_742053.1:p.Lys638=
NM_172057.2:c.892A= , LRG_288t3:c.892A= NP_742054.1:p.Lys298=
XM_011516185.1:c.1612A= XP_011514487.1:p.Lys538=
XM_011516186.1:c.1912A= XP_011514488.1:p.Lys638=
XM_011516185.2:c.1612A= XP_011514487.1:p.Lys538=
XM_011516186.3:c.1912A= XP_011514488.1:p.Lys638=
XM_017012195.1:c.1762A= XP_016867684.1:p.Lys588=
XM_017012196.1:c.1735A= XP_016867685.1:p.Lys579=
NM_000238.4:c.1912A= MANE Select NP_000229.1:p.Lys638=
NM_001204798.2:c.892A= NP_001191727.1:p.Lys298=
NM_172057.3:c.892A= NP_742054.1:p.Lys298=