Canonical Allele Identifier: CA1752416990
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150957490G= , CM000669.2:g.150957490G= GRCh38
NC_000007.13:g.150654578G= , CM000669.1:g.150654578G= GRCh37
NC_000007.12:g.150285511G= NCBI36
NG_008916.1:g.25437C= , LRG_288:g.25437C=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1762C=
ENST00000262186.10:c.929C= MANE Select ENSP00000262186.5:p.Pro310=
ENST00000262186.9:c.929C= ENSP00000262186.5:p.Pro310=
ENST00000430723.4:c.581C= ENSP00000387657.4:p.Pro194=
ENST00000532957.5:n.1152C=
NM_000238.3:c.929C= , LRG_288t1:c.929C= NP_000229.1:p.Pro310=
NM_172056.2:c.929C= , LRG_288t2:c.929C= NP_742053.1:p.Pro310=
XM_011516185.1:c.629C= XP_011514487.1:p.Pro210=
XM_011516186.1:c.929C= XP_011514488.1:p.Pro310=
XM_011516185.2:c.629C= XP_011514487.1:p.Pro210=
XM_011516186.3:c.929C= XP_011514488.1:p.Pro310=
XM_017012195.1:c.779C= XP_016867684.1:p.Pro260=
XM_017012196.1:c.752C= XP_016867685.1:p.Pro251=
NM_000238.4:c.929C= MANE Select NP_000229.1:p.Pro310=