Canonical Allele Identifier: CA1752410292
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951662T= , CM000669.2:g.150951662T= GRCh38
NC_000007.13:g.150648750T= , CM000669.1:g.150648750T= GRCh37
NC_000007.12:g.150279683T= NCBI36
NG_008916.1:g.31265A= , LRG_288:g.31265A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1029A=
ENST00000684241.1:n.2564A=
ENST00000262186.10:c.1731A= MANE Select ENSP00000262186.5:p.Pro577=
ENST00000330883.9:c.711A= ENSP00000328531.4:p.Pro237=
ENST00000262186.9:c.1731A= ENSP00000262186.5:p.Pro577=
ENST00000330883.8:c.711A= ENSP00000328531.4:p.Pro237=
ENST00000430723.4:c.1383A= ENSP00000387657.4:p.Pro461=
ENST00000461280.1:n.1018A=
ENST00000473610.5:n.1036A=
ENST00000532957.5:n.1954A=
NM_000238.3:c.1731A= , LRG_288t1:c.1731A= NP_000229.1:p.Pro577=
NM_001204798.1:c.711A= NP_001191727.1:p.Pro237=
NM_172056.2:c.1731A= , LRG_288t2:c.1731A= NP_742053.1:p.Pro577=
NM_172057.2:c.711A= , LRG_288t3:c.711A= NP_742054.1:p.Pro237=
XM_011516185.1:c.1431A= XP_011514487.1:p.Pro477=
XM_011516186.1:c.1731A= XP_011514488.1:p.Pro577=
XM_011516185.2:c.1431A= XP_011514487.1:p.Pro477=
XM_011516186.3:c.1731A= XP_011514488.1:p.Pro577=
XM_017012195.1:c.1581A= XP_016867684.1:p.Pro527=
XM_017012196.1:c.1554A= XP_016867685.1:p.Pro518=
NM_000238.4:c.1731A= MANE Select NP_000229.1:p.Pro577=
NM_001204798.2:c.711A= NP_001191727.1:p.Pro237=
NM_172057.3:c.711A= NP_742054.1:p.Pro237=