Canonical Allele Identifier: CA1752431861
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948882G= , CM000669.2:g.150948882G= GRCh38
NC_000007.13:g.150645970G= , CM000669.1:g.150645970G= GRCh37
NC_000007.12:g.150276903G= NCBI36
NG_008916.1:g.34045C= , LRG_288:g.34045C=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.3399C=
ENST00000262186.10:c.2566C= MANE Select ENSP00000262186.5:p.Leu856=
ENST00000330883.9:c.1546C= ENSP00000328531.4:p.Leu516=
ENST00000262186.9:c.2566C= ENSP00000262186.5:p.Leu856=
ENST00000330883.8:c.1546C= ENSP00000328531.4:p.Leu516=
NM_000238.3:c.2566C= , LRG_288t1:c.2566C= NP_000229.1:p.Leu856=
NM_172057.2:c.1546C= , LRG_288t3:c.1546C= NP_742054.1:p.Leu516=
XM_011516185.1:c.2266C= XP_011514487.1:p.Leu756=
XM_011516186.1:c.2566C= XP_011514488.1:p.Leu856=
XM_011516185.2:c.2266C= XP_011514487.1:p.Leu756=
XM_011516186.3:c.2566C= XP_011514488.1:p.Leu856=
XM_017012195.1:c.2416C= XP_016867684.1:p.Leu806=
XM_017012196.1:c.2389C= XP_016867685.1:p.Leu797=
NM_000238.4:c.2566C= MANE Select NP_000229.1:p.Leu856=
NM_172057.3:c.1546C= NP_742054.1:p.Leu516=