Canonical Allele Identifier: CA1752417018
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150957496A= , CM000669.2:g.150957496A= GRCh38
NC_000007.13:g.150654584A= , CM000669.1:g.150654584A= GRCh37
NC_000007.12:g.150285517A= NCBI36
NG_008916.1:g.25431T= , LRG_288:g.25431T=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1756T=
ENST00000262186.10:c.923T= MANE Select ENSP00000262186.5:p.Met308=
ENST00000262186.9:c.923T= ENSP00000262186.5:p.Met308=
ENST00000430723.4:c.575T= ENSP00000387657.4:p.Met192=
ENST00000532957.5:n.1146T=
NM_000238.3:c.923T= , LRG_288t1:c.923T= NP_000229.1:p.Met308=
NM_172056.2:c.923T= , LRG_288t2:c.923T= NP_742053.1:p.Met308=
XM_011516185.1:c.623T= XP_011514487.1:p.Met208=
XM_011516186.1:c.923T= XP_011514488.1:p.Met308=
XM_011516185.2:c.623T= XP_011514487.1:p.Met208=
XM_011516186.3:c.923T= XP_011514488.1:p.Met308=
XM_017012195.1:c.773T= XP_016867684.1:p.Met258=
XM_017012196.1:c.746T= XP_016867685.1:p.Met249=
NM_000238.4:c.923T= MANE Select NP_000229.1:p.Met308=