Canonical Allele Identifier: CA2685607981

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150958257-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958258del , CM000669.2:g.150958258del	GRCh38
NC_000007.13:g.150655346del , CM000669.1:g.150655346del	GRCh37
NC_000007.12:g.150286279del	NCBI36
NG_008916.1:g.24669del , LRG_288:g.24669del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1550del
ENST00000262186.10:c.717del MANE Select	ENSP00000262186.5:p.Pro240ArgfsTer?
ENST00000262186.9:c.717del	ENSP00000262186.5:p.Pro240ArgfsTer?
ENST00000430723.4:c.369del	ENSP00000387657.4:p.Pro124ArgfsTer?
ENST00000532957.5:n.940del
NM_000238.3:c.717del , LRG_288t1:c.717del	NP_000229.1:p.Pro240ArgfsTer?
NM_172056.2:c.717del , LRG_288t2:c.717del	NP_742053.1:p.Pro240ArgfsTer?
XM_011516185.1:c.417del	XP_011514487.1:p.Pro140ArgfsTer?
XM_011516186.1:c.717del	XP_011514488.1:p.Pro240ArgfsTer?
XM_011516185.2:c.417del	XP_011514487.1:p.Pro140ArgfsTer?
XM_011516186.3:c.717del	XP_011514488.1:p.Pro240ArgfsTer?
XM_017012195.1:c.567del	XP_016867684.1:p.Pro190ArgfsTer?
XM_017012196.1:c.540del	XP_016867685.1:p.Pro181ArgfsTer?
NM_000238.4:c.717del MANE Select	NP_000229.1:p.Pro240ArgfsTer?