Canonical Allele Identifier: CA369866029

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150974934-C-A
• MyVariant Identifiers: chr7:g.150672022C>A (hg19) ; chr7:g.150974934C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974934C>A , CM000669.2:g.150974934C>A	GRCh38
NC_000007.13:g.150672022C>A , CM000669.1:g.150672022C>A	GRCh37
NC_000007.12:g.150302955C>A	NCBI36
NG_008916.1:g.7993G>T , LRG_288:g.7993G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.84G>T MANE Select	ENSP00000262186.5:p.Lys28Asn
ENST00000262186.9:c.84G>T	ENSP00000262186.5:p.Lys28Asn
ENST00000430723.4:c.-94G>T	ENSP00000387657.4:n.-94G>T
ENST00000532957.5:n.307G>T
NM_000238.3:c.84G>T , LRG_288t1:c.84G>T	NP_000229.1:p.Lys28Asn
NM_172056.2:c.84G>T , LRG_288t2:c.84G>T	NP_742053.1:p.Lys28Asn
XM_011516186.1:c.84G>T	XP_011514488.1:p.Lys28Asn
XM_011516186.3:c.84G>T	XP_011514488.1:p.Lys28Asn
XM_017012196.1:c.-94G>T	XP_016867685.1:n.-94G>T
NM_000238.4:c.84G>T MANE Select	NP_000229.1:p.Lys28Asn