Canonical Allele Identifier: CA1752416980
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150957487A= , CM000669.2:g.150957487A= GRCh38
NC_000007.13:g.150654575A= , CM000669.1:g.150654575A= GRCh37
NC_000007.12:g.150285508A= NCBI36
NG_008916.1:g.25440T= , LRG_288:g.25440T=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1765T=
ENST00000262186.10:c.932T= MANE Select ENSP00000262186.5:p.Leu311=
ENST00000262186.9:c.932T= ENSP00000262186.5:p.Leu311=
ENST00000430723.4:c.584T= ENSP00000387657.4:p.Leu195=
ENST00000532957.5:n.1155T=
NM_000238.3:c.932T= , LRG_288t1:c.932T= NP_000229.1:p.Leu311=
NM_172056.2:c.932T= , LRG_288t2:c.932T= NP_742053.1:p.Leu311=
XM_011516185.1:c.632T= XP_011514487.1:p.Leu211=
XM_011516186.1:c.932T= XP_011514488.1:p.Leu311=
XM_011516185.2:c.632T= XP_011514487.1:p.Leu211=
XM_011516186.3:c.932T= XP_011514488.1:p.Leu311=
XM_017012195.1:c.782T= XP_016867684.1:p.Leu261=
XM_017012196.1:c.755T= XP_016867685.1:p.Leu252=
NM_000238.4:c.932T= MANE Select NP_000229.1:p.Leu311=