Canonical Allele Identifier: CA1752417692
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150958064C= , CM000669.2:g.150958064C= GRCh38
NC_000007.13:g.150655152C= , CM000669.1:g.150655152C= GRCh37
NC_000007.12:g.150286085C= NCBI36
NG_008916.1:g.24863G= , LRG_288:g.24863G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1744G=
ENST00000262186.10:c.911G= MANE Select ENSP00000262186.5:p.Ser304=
ENST00000262186.9:c.911G= ENSP00000262186.5:p.Ser304=
ENST00000430723.4:c.563G= ENSP00000387657.4:p.Ser188=
ENST00000532957.5:n.1134G=
NM_000238.3:c.911G= , LRG_288t1:c.911G= NP_000229.1:p.Ser304=
NM_172056.2:c.911G= , LRG_288t2:c.911G= NP_742053.1:p.Ser304=
XM_011516185.1:c.611G= XP_011514487.1:p.Ser204=
XM_011516186.1:c.911G= XP_011514488.1:p.Ser304=
XM_011516185.2:c.611G= XP_011514487.1:p.Ser204=
XM_011516186.3:c.911G= XP_011514488.1:p.Ser304=
XM_017012195.1:c.761G= XP_016867684.1:p.Ser254=
XM_017012196.1:c.734G= XP_016867685.1:p.Ser245=
NM_000238.4:c.911G= MANE Select NP_000229.1:p.Ser304=