Canonical Allele Identifier: CA1752418462
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150958338C= , CM000669.2:g.150958338C= GRCh38
NC_000007.13:g.150655426C= , CM000669.1:g.150655426C= GRCh37
NC_000007.12:g.150286359C= NCBI36
NG_008916.1:g.24589G= , LRG_288:g.24589G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1470G=
ENST00000262186.10:c.637G= MANE Select ENSP00000262186.5:p.Asp213=
ENST00000262186.9:c.637G= ENSP00000262186.5:p.Asp213=
ENST00000430723.4:c.289G= ENSP00000387657.4:p.Asp97=
ENST00000532957.5:n.860G=
NM_000238.3:c.637G= , LRG_288t1:c.637G= NP_000229.1:p.Asp213=
NM_172056.2:c.637G= , LRG_288t2:c.637G= NP_742053.1:p.Asp213=
XM_011516185.1:c.337G= XP_011514487.1:p.Asp113=
XM_011516186.1:c.637G= XP_011514488.1:p.Asp213=
XM_011516185.2:c.337G= XP_011514487.1:p.Asp113=
XM_011516186.3:c.637G= XP_011514488.1:p.Asp213=
XM_017012195.1:c.487G= XP_016867684.1:p.Asp163=
XM_017012196.1:c.460G= XP_016867685.1:p.Asp154=
NM_000238.4:c.637G= MANE Select NP_000229.1:p.Asp213=