Canonical Allele Identifier: CA2695208624

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957430_150957440del , CM000669.2:g.150957430_150957440del	GRCh38
NC_000007.13:g.150654518_150654528del , CM000669.1:g.150654518_150654528del	GRCh37
NC_000007.12:g.150285451_150285461del	NCBI36
NG_008916.1:g.25489_25499del , LRG_288:g.25489_25499del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1814_1824del
ENST00000262186.10:c.981_991del MANE Select	ENSP00000262186.5:p.Tyr327Ter
ENST00000262186.9:c.981_991del	ENSP00000262186.5:p.Tyr327Ter
ENST00000430723.4:c.633_643del	ENSP00000387657.4:p.Tyr211Ter
ENST00000532957.5:n.1204_1214del
NM_000238.3:c.981_991del , LRG_288t1:c.981_991del	NP_000229.1:p.Tyr327Ter
NM_172056.2:c.981_991del , LRG_288t2:c.981_991del	NP_742053.1:p.Tyr327Ter
XM_011516185.1:c.681_691del	XP_011514487.1:p.Tyr227Ter
XM_011516186.1:c.981_991del	XP_011514488.1:p.Tyr327Ter
XM_011516185.2:c.681_691del	XP_011514487.1:p.Tyr227Ter
XM_011516186.3:c.981_991del	XP_011514488.1:p.Tyr327Ter
XM_017012195.1:c.831_841del	XP_016867684.1:p.Tyr277Ter
XM_017012196.1:c.804_814del	XP_016867685.1:p.Tyr268Ter
NM_000238.4:c.981_991del MANE Select	NP_000229.1:p.Tyr327Ter