Canonical Allele Identifier: CA369861818
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150957461A>C , CM000669.2:g.150957461A>C GRCh38
NC_000007.13:g.150654549A>C , CM000669.1:g.150654549A>C GRCh37
NC_000007.12:g.150285482A>C NCBI36
NG_008916.1:g.25466T>G , LRG_288:g.25466T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.1791T>G
ENST00000262186.10:c.958T>G MANE Select ENSP00000262186.5:p.Ser320Ala
ENST00000262186.9:c.958T>G ENSP00000262186.5:p.Ser320Ala
ENST00000430723.4:c.610T>G ENSP00000387657.4:p.Ser204Ala
ENST00000532957.5:n.1181T>G
NM_000238.3:c.958T>G , LRG_288t1:c.958T>G NP_000229.1:p.Ser320Ala
NM_172056.2:c.958T>G , LRG_288t2:c.958T>G NP_742053.1:p.Ser320Ala
XM_011516185.1:c.658T>G XP_011514487.1:p.Ser220Ala
XM_011516186.1:c.958T>G XP_011514488.1:p.Ser320Ala
XM_011516185.2:c.658T>G XP_011514487.1:p.Ser220Ala
XM_011516186.3:c.958T>G XP_011514488.1:p.Ser320Ala
XM_017012195.1:c.808T>G XP_016867684.1:p.Ser270Ala
XM_017012196.1:c.781T>G XP_016867685.1:p.Ser261Ala
NM_000238.4:c.958T>G MANE Select NP_000229.1:p.Ser320Ala