Canonical Allele Identifier: CA2685602515
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948413_150948446del , CM000669.2:g.150948413_150948446del GRCh38
NC_000007.13:g.150645501_150645534del , CM000669.1:g.150645501_150645534del GRCh37
NC_000007.12:g.150276434_150276467del NCBI36
NG_008916.1:g.34481_34514del , LRG_288:g.34481_34514del

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.3523_3525+31del
ENST00000262186.10:c.2690_2692+31del
ENST00000330883.9:c.1670_1672+31del
ENST00000262186.9:c.2690_2692+31del
ENST00000330883.8:c.1670_1672+31del
NM_000238.3:c.2690_2692+31del , LRG_288t1:c.2690_2692+31del
NM_172057.2:c.1670_1672+31del , LRG_288t3:c.1670_1672+31del
XM_011516185.1:c.2390_2392+31del
XM_011516186.1:c.2690_2692+31del
XM_011516185.2:c.2390_2392+31del
XM_011516186.3:c.2690_2692+31del
XM_017012195.1:c.2540_2542+31del
XM_017012196.1:c.2513_2515+31del
NM_000238.4:c.2690_2692+31del
NM_172057.3:c.1670_1672+31del