Canonical Allele Identifier: CA1752419059

Gene: KCNH2

Linked Data

• dbSNP Id: rs1801471444

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958681_150958689del , CM000669.2:g.150958681_150958689del	GRCh38
NC_000007.13:g.150655769_150655777del , CM000669.1:g.150655769_150655777del	GRCh37
NC_000007.12:g.150286702_150286710del	NCBI36
NG_008916.1:g.24238_24246del , LRG_288:g.24238_24246del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1306-187_1306-179del
ENST00000262186.10:c.473-187_473-179del MANE Select	ENSP00000262186.5:n.473-187_473-179del
ENST00000262186.9:c.473-187_473-179del	ENSP00000262186.5:n.473-187_473-179del
ENST00000430723.4:c.235-297_235-289del	ENSP00000387657.4:n.235-297_235-289del
ENST00000532957.5:n.696-187_696-179del
NM_000238.3:c.473-187_473-179del , LRG_288t1:c.473-187_473-179del	NP_000229.1:n.473-187_473-179del
NM_172056.2:c.473-187_473-179del , LRG_288t2:c.473-187_473-179del	NP_742053.1:n.473-187_473-179del
XM_011516185.1:c.173-187_173-179del	XP_011514487.1:n.173-187_173-179del
XM_011516186.1:c.473-187_473-179del	XP_011514488.1:n.473-187_473-179del
XM_011516185.2:c.173-187_173-179del	XP_011514487.1:n.173-187_173-179del
XM_011516186.3:c.473-187_473-179del	XP_011514488.1:n.473-187_473-179del
XM_017012195.1:c.323-187_323-179del	XP_016867684.1:n.323-187_323-179del
XM_017012196.1:c.296-187_296-179del	XP_016867685.1:n.296-187_296-179del
NM_000238.4:c.473-187_473-179del MANE Select	NP_000229.1:n.473-187_473-179del