Canonical Allele Identifier: CA458871505

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 456896
• ClinVar RCV Id: RCV000551353
• dbSNP Id: rs1554425781
• gnomAD v4: 7-150951557-C-T
• MyVariant Identifiers: chr7:g.150648645C>T (hg19) ; chr7:g.150951557C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951557C>T , CM000669.2:g.150951557C>T	GRCh38
NC_000007.13:g.150648645C>T , CM000669.1:g.150648645C>T	GRCh37
NC_000007.12:g.150279578C>T	NCBI36
NG_008916.1:g.31370G>A , LRG_288:g.31370G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1134G>A
ENST00000684241.1:n.2669G>A
ENST00000262186.10:c.1836G>A MANE Select	ENSP00000262186.5:p.Val612=
ENST00000330883.9:c.816G>A	ENSP00000328531.4:p.Val272=
ENST00000262186.9:c.1836G>A	ENSP00000262186.5:p.Val612=
ENST00000330883.8:c.816G>A	ENSP00000328531.4:p.Val272=
ENST00000430723.4:c.1488G>A	ENSP00000387657.4:p.Val496=
ENST00000461280.1:n.1123G>A
ENST00000473610.5:n.1141G>A
ENST00000532957.5:n.2059G>A
NM_000238.3:c.1836G>A , LRG_288t1:c.1836G>A	NP_000229.1:p.Val612=
NM_001204798.1:c.816G>A	NP_001191727.1:p.Val272=
NM_172056.2:c.1836G>A , LRG_288t2:c.1836G>A	NP_742053.1:p.Val612=
NM_172057.2:c.816G>A , LRG_288t3:c.816G>A	NP_742054.1:p.Val272=
XM_011516185.1:c.1536G>A	XP_011514487.1:p.Val512=
XM_011516186.1:c.1836G>A	XP_011514488.1:p.Val612=
XM_011516185.2:c.1536G>A	XP_011514487.1:p.Val512=
XM_011516186.3:c.1836G>A	XP_011514488.1:p.Val612=
XM_017012195.1:c.1686G>A	XP_016867684.1:p.Val562=
XM_017012196.1:c.1659G>A	XP_016867685.1:p.Val553=
NM_000238.4:c.1836G>A MANE Select	NP_000229.1:p.Val612=
NM_001204798.2:c.816G>A	NP_001191727.1:p.Val272=
NM_172057.3:c.816G>A	NP_742054.1:p.Val272=