Canonical Allele Identifier: CA1752417722
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150958072G= , CM000669.2:g.150958072G= GRCh38
NC_000007.13:g.150655160G= , CM000669.1:g.150655160G= GRCh37
NC_000007.12:g.150286093G= NCBI36
NG_008916.1:g.24855C= , LRG_288:g.24855C=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1736C=
ENST00000262186.10:c.903C= MANE Select ENSP00000262186.5:p.Arg301=
ENST00000262186.9:c.903C= ENSP00000262186.5:p.Arg301=
ENST00000430723.4:c.555C= ENSP00000387657.4:p.Arg185=
ENST00000532957.5:n.1126C=
NM_000238.3:c.903C= , LRG_288t1:c.903C= NP_000229.1:p.Arg301=
NM_172056.2:c.903C= , LRG_288t2:c.903C= NP_742053.1:p.Arg301=
XM_011516185.1:c.603C= XP_011514487.1:p.Arg201=
XM_011516186.1:c.903C= XP_011514488.1:p.Arg301=
XM_011516185.2:c.603C= XP_011514487.1:p.Arg201=
XM_011516186.3:c.903C= XP_011514488.1:p.Arg301=
XM_017012195.1:c.753C= XP_016867684.1:p.Arg251=
XM_017012196.1:c.726C= XP_016867685.1:p.Arg242=
NM_000238.4:c.903C= MANE Select NP_000229.1:p.Arg301=