Canonical Allele Identifier: CA2695208740

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952662_150952911del , CM000669.2:g.150952662_150952911del	GRCh38
NC_000007.13:g.150649750_150649999del , CM000669.1:g.150649750_150649999del	GRCh37
NC_000007.12:g.150280683_150280932del	NCBI36
NG_008916.1:g.30021_30270del , LRG_288:g.30021_30270del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.427-53_623del
ENST00000684241.1:n.1962-53_2158del
ENST00000262186.10:c.1129-53_1325del
ENST00000330883.9:c.109-53_305del
ENST00000262186.9:c.1129-53_1325del
ENST00000330883.8:c.109-53_305del
ENST00000430723.4:c.781-53_977del
ENST00000461280.1:n.416-53_612del
ENST00000473610.5:n.434-53_630del
ENST00000532957.5:n.1352-53_1548del
NM_000238.3:c.1129-53_1325del , LRG_288t1:c.1129-53_1325del
NM_001204798.1:c.109-53_305del
NM_172056.2:c.1129-53_1325del , LRG_288t2:c.1129-53_1325del
NM_172057.2:c.109-53_305del , LRG_288t3:c.109-53_305del
XM_011516185.1:c.829-53_1025del
XM_011516186.1:c.1129-53_1325del
XM_011516185.2:c.829-53_1025del
XM_011516186.3:c.1129-53_1325del
XM_017012195.1:c.979-53_1175del
XM_017012196.1:c.952-53_1148del
NM_000238.4:c.1129-53_1325del
NM_001204798.2:c.109-53_305del
NM_172057.3:c.109-53_305del