Canonical Allele Identifier: CA1752427209
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150946821T= , CM000669.2:g.150946821T= GRCh38
NC_000007.13:g.150643909T= , CM000669.1:g.150643909T= GRCh37
NC_000007.12:g.150274842T= NCBI36
NG_008916.1:g.36106A= , LRG_288:g.36106A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.4163+56A=
ENST00000262186.10:c.3330+56A= MANE Select ENSP00000262186.5:n.3330+56A=
ENST00000330883.9:c.2310+56A= ENSP00000328531.4:n.2310+56A=
ENST00000262186.9:c.3330+56A= ENSP00000262186.5:n.3330+56A=
ENST00000330883.8:c.2310+56A= ENSP00000328531.4:n.2310+56A=
NM_000238.3:c.3330+56A= , LRG_288t1:c.3330+56A= NP_000229.1:n.3330+56A=
NM_172057.2:c.2310+56A= , LRG_288t3:c.2310+56A= NP_742054.1:n.2310+56A=
XM_011516185.1:c.3030+56A= XP_011514487.1:n.3030+56A=
XM_011516185.2:c.3030+56A= XP_011514487.1:n.3030+56A=
XM_017012195.1:c.3180+56A= XP_016867684.1:n.3180+56A=
XM_017012196.1:c.3153+56A= XP_016867685.1:n.3153+56A=
NM_000238.4:c.3330+56A= MANE Select NP_000229.1:n.3330+56A=
NM_172057.3:c.2310+56A= NP_742054.1:n.2310+56A=