Canonical Allele Identifier: CA1752418475
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150958341G= , CM000669.2:g.150958341G= GRCh38
NC_000007.13:g.150655429G= , CM000669.1:g.150655429G= GRCh37
NC_000007.12:g.150286362G= NCBI36
NG_008916.1:g.24586C= , LRG_288:g.24586C=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1467C=
ENST00000262186.10:c.634C= MANE Select ENSP00000262186.5:p.Leu212=
ENST00000262186.9:c.634C= ENSP00000262186.5:p.Leu212=
ENST00000430723.4:c.286C= ENSP00000387657.4:p.Leu96=
ENST00000532957.5:n.857C=
NM_000238.3:c.634C= , LRG_288t1:c.634C= NP_000229.1:p.Leu212=
NM_172056.2:c.634C= , LRG_288t2:c.634C= NP_742053.1:p.Leu212=
XM_011516185.1:c.334C= XP_011514487.1:p.Leu112=
XM_011516186.1:c.634C= XP_011514488.1:p.Leu212=
XM_011516185.2:c.334C= XP_011514487.1:p.Leu112=
XM_011516186.3:c.634C= XP_011514488.1:p.Leu212=
XM_017012195.1:c.484C= XP_016867684.1:p.Leu162=
XM_017012196.1:c.457C= XP_016867685.1:p.Leu153=
NM_000238.4:c.634C= MANE Select NP_000229.1:p.Leu212=