Canonical Allele Identifier: CA835204333

Gene: KCNH2

Linked Data

• dbSNP Id: rs1390610216
• gnomAD v3: 7-150958614-AC-A
• gnomAD v4: 7-150958614-AC-A
• MyVariant Identifiers: chr7:g.150655703del (hg19) ; chr7:g.150958615del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958620del , CM000669.2:g.150958620del	GRCh38
NC_000007.13:g.150655708del , CM000669.1:g.150655708del	GRCh37
NC_000007.12:g.150286641del	NCBI36
NG_008916.1:g.24312del , LRG_288:g.24312del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1306-113del
ENST00000262186.10:c.473-113del MANE Select	ENSP00000262186.5:n.473-113del
ENST00000262186.9:c.473-113del	ENSP00000262186.5:n.473-113del
ENST00000430723.4:c.235-223del	ENSP00000387657.4:n.235-223del
ENST00000532957.5:n.696-113del
NM_000238.3:c.473-113del , LRG_288t1:c.473-113del	NP_000229.1:n.473-113del
NM_172056.2:c.473-113del , LRG_288t2:c.473-113del	NP_742053.1:n.473-113del
XM_011516185.1:c.173-113del	XP_011514487.1:n.173-113del
XM_011516186.1:c.473-113del	XP_011514488.1:n.473-113del
XM_011516185.2:c.173-113del	XP_011514487.1:n.173-113del
XM_011516186.3:c.473-113del	XP_011514488.1:n.473-113del
XM_017012195.1:c.323-113del	XP_016867684.1:n.323-113del
XM_017012196.1:c.296-113del	XP_016867685.1:n.296-113del
NM_000238.4:c.473-113del MANE Select	NP_000229.1:n.473-113del