Canonical Allele Identifier: CA1752434943
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951458C= , CM000669.2:g.150951458C= GRCh38
NC_000007.13:g.150648546C= , CM000669.1:g.150648546C= GRCh37
NC_000007.12:g.150279479C= NCBI36
NG_008916.1:g.31469G= , LRG_288:g.31469G=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1233G=
ENST00000683359.1:n.59G=
ENST00000684241.1:n.2768G=
ENST00000262186.10:c.1935G= MANE Select ENSP00000262186.5:p.Met645=
ENST00000330883.9:c.915G= ENSP00000328531.4:p.Met305=
ENST00000262186.9:c.1935G= ENSP00000262186.5:p.Met645=
ENST00000330883.8:c.915G= ENSP00000328531.4:p.Met305=
ENST00000430723.4:c.1587G= ENSP00000387657.4:p.Met529=
ENST00000461280.1:n.1222G=
ENST00000473610.5:n.1240G=
ENST00000532957.5:n.2158G=
NM_000238.3:c.1935G= , LRG_288t1:c.1935G= NP_000229.1:p.Met645=
NM_001204798.1:c.915G= NP_001191727.1:p.Met305=
NM_172056.2:c.1935G= , LRG_288t2:c.1935G= NP_742053.1:p.Met645=
NM_172057.2:c.915G= , LRG_288t3:c.915G= NP_742054.1:p.Met305=
XM_011516185.1:c.1635G= XP_011514487.1:p.Met545=
XM_011516186.1:c.1935G= XP_011514488.1:p.Met645=
XM_011516185.2:c.1635G= XP_011514487.1:p.Met545=
XM_011516186.3:c.1935G= XP_011514488.1:p.Met645=
XM_017012195.1:c.1785G= XP_016867684.1:p.Met595=
XM_017012196.1:c.1758G= XP_016867685.1:p.Met586=
NM_000238.4:c.1935G= MANE Select NP_000229.1:p.Met645=
NM_001204798.2:c.915G= NP_001191727.1:p.Met305=
NM_172057.3:c.915G= NP_742054.1:p.Met305=