Canonical Allele Identifier: CA2685600716

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150948785-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948790_150948791del , CM000669.2:g.150948790_150948791del	GRCh38
NC_000007.13:g.150645878_150645879del , CM000669.1:g.150645878_150645879del	GRCh37
NC_000007.12:g.150276811_150276812del	NCBI36
NG_008916.1:g.34140_34141del , LRG_288:g.34140_34141del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3425+69_3425+70del
ENST00000262186.10:c.2592+69_2592+70del MANE Select	ENSP00000262186.5:n.2592+69_2592+70del
ENST00000330883.9:c.1572+69_1572+70del	ENSP00000328531.4:n.1572+69_1572+70del
ENST00000262186.9:c.2592+69_2592+70del	ENSP00000262186.5:n.2592+69_2592+70del
ENST00000330883.8:c.1572+69_1572+70del	ENSP00000328531.4:n.1572+69_1572+70del
NM_000238.3:c.2592+69_2592+70del , LRG_288t1:c.2592+69_2592+70del	NP_000229.1:n.2592+69_2592+70del
NM_172057.2:c.1572+69_1572+70del , LRG_288t3:c.1572+69_1572+70del	NP_742054.1:n.1572+69_1572+70del
XM_011516185.1:c.2292+69_2292+70del	XP_011514487.1:n.2292+69_2292+70del
XM_011516186.1:c.2592+69_2592+70del	XP_011514488.1:n.2592+69_2592+70del
XM_011516185.2:c.2292+69_2292+70del	XP_011514487.1:n.2292+69_2292+70del
XM_011516186.3:c.2592+69_2592+70del	XP_011514488.1:n.2592+69_2592+70del
XM_017012195.1:c.2442+69_2442+70del	XP_016867684.1:n.2442+69_2442+70del
XM_017012196.1:c.2415+69_2415+70del	XP_016867685.1:n.2415+69_2415+70del
NM_000238.4:c.2592+69_2592+70del MANE Select	NP_000229.1:n.2592+69_2592+70del
NM_172057.3:c.1572+69_1572+70del	NP_742054.1:n.1572+69_1572+70del