Canonical Allele Identifier: CA1752425635
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150945408G= , CM000669.2:g.150945408G= GRCh38
NC_000007.13:g.150642496G= , CM000669.1:g.150642496G= GRCh37
NC_000007.12:g.150273429G= NCBI36
NG_008916.1:g.37519C= , LRG_288:g.37519C=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.4270C=
ENST00000262186.10:c.3437C= MANE Select ENSP00000262186.5:p.Thr1146=
ENST00000330883.9:c.2417C= ENSP00000328531.4:p.Thr806=
ENST00000262186.9:c.3437C= ENSP00000262186.5:p.Thr1146=
ENST00000330883.8:c.2417C= ENSP00000328531.4:p.Thr806=
NM_000238.3:c.3437C= , LRG_288t1:c.3437C= NP_000229.1:p.Thr1146=
NM_172057.2:c.2417C= , LRG_288t3:c.2417C= NP_742054.1:p.Thr806=
XM_011516185.1:c.3137C= XP_011514487.1:p.Thr1046=
XM_011516185.2:c.3137C= XP_011514487.1:p.Thr1046=
XM_017012195.1:c.3287C= XP_016867684.1:p.Thr1096=
XM_017012196.1:c.3260C= XP_016867685.1:p.Thr1087=
NM_000238.4:c.3437C= MANE Select NP_000229.1:p.Thr1146=
NM_172057.3:c.2417C= NP_742054.1:p.Thr806=