Canonical Allele Identifier: CA1752417696
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150958065T= , CM000669.2:g.150958065T= GRCh38
NC_000007.13:g.150655153T= , CM000669.1:g.150655153T= GRCh37
NC_000007.12:g.150286086T= NCBI36
NG_008916.1:g.24862A= , LRG_288:g.24862A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1743A=
ENST00000262186.10:c.910A= MANE Select ENSP00000262186.5:p.Ser304=
ENST00000262186.9:c.910A= ENSP00000262186.5:p.Ser304=
ENST00000430723.4:c.562A= ENSP00000387657.4:p.Ser188=
ENST00000532957.5:n.1133A=
NM_000238.3:c.910A= , LRG_288t1:c.910A= NP_000229.1:p.Ser304=
NM_172056.2:c.910A= , LRG_288t2:c.910A= NP_742053.1:p.Ser304=
XM_011516185.1:c.610A= XP_011514487.1:p.Ser204=
XM_011516186.1:c.910A= XP_011514488.1:p.Ser304=
XM_011516185.2:c.610A= XP_011514487.1:p.Ser204=
XM_011516186.3:c.910A= XP_011514488.1:p.Ser304=
XM_017012195.1:c.760A= XP_016867684.1:p.Ser254=
XM_017012196.1:c.733A= XP_016867685.1:p.Ser245=
NM_000238.4:c.910A= MANE Select NP_000229.1:p.Ser304=