Canonical Allele Identifier: CA369862356

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150958152-T-A
• MyVariant Identifiers: chr7:g.150655240T>A (hg19) ; chr7:g.150958152T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958152T>A , CM000669.2:g.150958152T>A	GRCh38
NC_000007.13:g.150655240T>A , CM000669.1:g.150655240T>A	GRCh37
NC_000007.12:g.150286173T>A	NCBI36
NG_008916.1:g.24775A>T , LRG_288:g.24775A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1656A>T
ENST00000262186.10:c.823A>T MANE Select	ENSP00000262186.5:p.Ser275Cys
ENST00000262186.9:c.823A>T	ENSP00000262186.5:p.Ser275Cys
ENST00000430723.4:c.475A>T	ENSP00000387657.4:p.Ser159Cys
ENST00000532957.5:n.1046A>T
NM_000238.3:c.823A>T , LRG_288t1:c.823A>T	NP_000229.1:p.Ser275Cys
NM_172056.2:c.823A>T , LRG_288t2:c.823A>T	NP_742053.1:p.Ser275Cys
XM_011516185.1:c.523A>T	XP_011514487.1:p.Ser175Cys
XM_011516186.1:c.823A>T	XP_011514488.1:p.Ser275Cys
XM_011516185.2:c.523A>T	XP_011514487.1:p.Ser175Cys
XM_011516186.3:c.823A>T	XP_011514488.1:p.Ser275Cys
XM_017012195.1:c.673A>T	XP_016867684.1:p.Ser225Cys
XM_017012196.1:c.646A>T	XP_016867685.1:p.Ser216Cys
NM_000238.4:c.823A>T MANE Select	NP_000229.1:p.Ser275Cys