Canonical Allele Identifier: CA369851995

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150946914-C-T
• MyVariant Identifiers: chr7:g.150644002C>T (hg19) ; chr7:g.150946914C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150946914C>T , CM000669.2:g.150946914C>T	GRCh38
NC_000007.13:g.150644002C>T , CM000669.1:g.150644002C>T	GRCh37
NC_000007.12:g.150274935C>T	NCBI36
NG_008916.1:g.36013G>A , LRG_288:g.36013G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.4126G>A
ENST00000262186.10:c.3293G>A MANE Select	ENSP00000262186.5:p.Ser1098Asn
ENST00000330883.9:c.2273G>A	ENSP00000328531.4:p.Ser758Asn
ENST00000262186.9:c.3293G>A	ENSP00000262186.5:p.Ser1098Asn
ENST00000330883.8:c.2273G>A	ENSP00000328531.4:p.Ser758Asn
NM_000238.3:c.3293G>A , LRG_288t1:c.3293G>A	NP_000229.1:p.Ser1098Asn
NM_172057.2:c.2273G>A , LRG_288t3:c.2273G>A	NP_742054.1:p.Ser758Asn
XM_011516185.1:c.2993G>A	XP_011514487.1:p.Ser998Asn
XM_011516185.2:c.2993G>A	XP_011514487.1:p.Ser998Asn
XM_017012195.1:c.3143G>A	XP_016867684.1:p.Ser1048Asn
XM_017012196.1:c.3116G>A	XP_016867685.1:p.Ser1039Asn
NM_000238.4:c.3293G>A MANE Select	NP_000229.1:p.Ser1098Asn
NM_172057.3:c.2273G>A	NP_742054.1:p.Ser758Asn