Canonical Allele Identifier: CA1752427206
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150946818G= , CM000669.2:g.150946818G= GRCh38
NC_000007.13:g.150643906G= , CM000669.1:g.150643906G= GRCh37
NC_000007.12:g.150274839G= NCBI36
NG_008916.1:g.36109C= , LRG_288:g.36109C=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.4163+59C=
ENST00000262186.10:c.3330+59C= MANE Select ENSP00000262186.5:n.3330+59C=
ENST00000330883.9:c.2310+59C= ENSP00000328531.4:n.2310+59C=
ENST00000262186.9:c.3330+59C= ENSP00000262186.5:n.3330+59C=
ENST00000330883.8:c.2310+59C= ENSP00000328531.4:n.2310+59C=
NM_000238.3:c.3330+59C= , LRG_288t1:c.3330+59C= NP_000229.1:n.3330+59C=
NM_172057.2:c.2310+59C= , LRG_288t3:c.2310+59C= NP_742054.1:n.2310+59C=
XM_011516185.1:c.3030+59C= XP_011514487.1:n.3030+59C=
XM_011516185.2:c.3030+59C= XP_011514487.1:n.3030+59C=
XM_017012195.1:c.3180+59C= XP_016867684.1:n.3180+59C=
XM_017012196.1:c.3153+59C= XP_016867685.1:n.3153+59C=
NM_000238.4:c.3330+59C= MANE Select NP_000229.1:n.3330+59C=
NM_172057.3:c.2310+59C= NP_742054.1:n.2310+59C=