Canonical Allele Identifier: CA1752429832
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150947635T= , CM000669.2:g.150947635T= GRCh38
NC_000007.13:g.150644723T= , CM000669.1:g.150644723T= GRCh37
NC_000007.12:g.150275656T= NCBI36
NG_008916.1:g.35292A= , LRG_288:g.35292A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.3769A=
ENST00000262186.10:c.2936A= MANE Select ENSP00000262186.5:p.Lys979=
ENST00000330883.9:c.1916A= ENSP00000328531.4:p.Lys639=
ENST00000262186.9:c.2936A= ENSP00000262186.5:p.Lys979=
ENST00000330883.8:c.1916A= ENSP00000328531.4:p.Lys639=
NM_000238.3:c.2936A= , LRG_288t1:c.2936A= NP_000229.1:p.Lys979=
NM_172057.2:c.1916A= , LRG_288t3:c.1916A= NP_742054.1:p.Lys639=
XM_011516185.1:c.2636A= XP_011514487.1:p.Lys879=
XM_011516186.1:c.*16A= XP_011514488.1:n.*16A=
XM_011516185.2:c.2636A= XP_011514487.1:p.Lys879=
XM_011516186.3:c.*16A= XP_011514488.1:n.*16A=
XM_017012195.1:c.2786A= XP_016867684.1:p.Lys929=
XM_017012196.1:c.2759A= XP_016867685.1:p.Lys920=
NM_000238.4:c.2936A= MANE Select NP_000229.1:p.Lys979=
NM_172057.3:c.1916A= NP_742054.1:p.Lys639=